Linked Data
ClinVar Variation Id:
555857
ClinVar RCV Id:
RCV000671765
dbSNP Id:
rs1373154561
gnomAD v3:
13-20189370-A-G
gnomAD v4:
13-20189370-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189370A>G , CM000675.2:g.20189370A>G | GRCh38 |
| NC_000013.10:g.20763509A>G , CM000675.1:g.20763509A>G | GRCh37 |
| NC_000013.9:g.19661509A>G | NCBI36 |
| NG_008358.1:g.8606T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.212T>C | ENSP00000372295.1:p.Ile71Thr | |
| ENST00000382848.5:c.212T>C MANE Select | ENSP00000372299.4:p.Ile71Thr | |
| ENST00000382844.1:c.212T>C | ENSP00000372295.1:p.Ile71Thr | |
| ENST00000382848.4:c.212T>C | ENSP00000372299.4:p.Ile71Thr | |
| NM_004004.5:c.212T>C | NP_003995.2:p.Ile71Thr | |
| XM_011535049.1:c.212T>C | XP_011533351.1:p.Ile71Thr | |
| XM_011535049.2:c.212T>C | XP_011533351.1:p.Ile71Thr | |
| NM_004004.6:c.212T>C MANE Select | NP_003995.2:p.Ile71Thr |