Linked Data
ClinVar Variation Id:
188131
dbSNP Id:
rs756906403
ExAC:
16:23632690 C / G
gnomAD v2:
16-23632690-C-G
gnomAD v3:
16-23621369-C-G
gnomAD v4:
16-23621369-C-G
PubMed:
PMID:26283626
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23621369C>G , CM000678.2:g.23621369C>G | GRCh38 |
| NC_000016.9:g.23632690C>G , CM000678.1:g.23632690C>G | GRCh37 |
| NC_000016.8:g.23540191C>G | NCBI36 |
| NG_007406.1:g.24989G>C , LRG_308:g.24989G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.3112G>C | ENSP00000460666.3:p.Val1038Leu | |
| ENST00000565038.2:c.*587G>C | ENSP00000459882.2:n.*587G>C | |
| ENST00000566069.6:c.3106G>C | ENSP00000459237.2:p.Val1036Leu | |
| ENST00000697377.2:c.2950G>C | ENSP00000513286.2:p.Val984Leu | |
| ENST00000697379.2:c.3112G>C | ENSP00000513287.2:p.Val1038Leu | |
| ENST00000561514.2:c.2221G>C | ENSP00000460666.2:p.Val741Leu | |
| ENST00000697374.1:c.2221G>C | ENSP00000513284.1:p.Val741Leu | |
| ENST00000697375.1:n.4453G>C | ||
| ENST00000697376.1:c.2221G>C | ENSP00000513285.1:p.Val741Leu | |
| ENST00000697377.1:c.2059G>C | ENSP00000513286.1:p.Val687Leu | |
| ENST00000697378.1:n.3626G>C | ||
| ENST00000697379.1:c.2221G>C | ENSP00000513287.1:p.Val741Leu | |
| ENST00000697380.1:n.2398G>C | ||
| ENST00000697381.1:n.1801G>C | ||
| ENST00000697382.1:c.2221G>C | ENSP00000513288.1:p.Val741Leu | |
| ENST00000697383.1:c.640G>C | ENSP00000513289.1:p.Val214Leu | |
| ENST00000261584.9:c.3106G>C MANE Select | ENSP00000261584.4:p.Val1036Leu | |
| ENST00000261584.8:c.3106G>C | ENSP00000261584.4:p.Val1036Leu | |
| ENST00000566069.5:c.21G>C | ||
| ENST00000568219.5:c.2221G>C | ENSP00000454703.2:p.Val741Leu | |
| NM_024675.3:c.3106G>C , LRG_308t1:c.3106G>C | NP_078951.2:p.Val1036Leu | |
| XM_011545946.1:c.3112G>C | XP_011544248.1:p.Val1038Leu | |
| XM_011545947.1:c.3112G>C | XP_011544249.1:p.Val1038Leu | |
| XM_011545948.1:c.2221G>C | XP_011544250.1:p.Val741Leu | |
| XR_950851.1:n.3902G>C | ||
| XM_011545946.2:c.3112G>C | XP_011544248.1:p.Val1038Leu | |
| XM_011545947.2:c.3112G>C | XP_011544249.1:p.Val1038Leu | |
| XM_011545948.2:c.2221G>C | XP_011544250.1:p.Val741Leu | |
| XM_017023671.1:c.3112G>C | XP_016879160.1:p.Val1038Leu | |
| XM_017023672.2:c.3106G>C | XP_016879161.1:p.Val1036Leu | |
| XM_017023673.2:c.3106G>C | XP_016879162.1:p.Val1036Leu | |
| NM_024675.4:c.3106G>C MANE Select | NP_078951.2:p.Val1036Leu |