Linked Data
dbSNP Id:
rs1193926371
gnomAD v2:
13-20763751-G-C
gnomAD v3:
13-20189612-G-C
gnomAD v4:
13-20189612-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189612G>C , CM000675.2:g.20189612G>C | GRCh38 |
| NC_000013.10:g.20763751G>C , CM000675.1:g.20763751G>C | GRCh37 |
| NC_000013.9:g.19661751G>C | NCBI36 |
| NG_008358.1:g.8364C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.-31C>G | ENSP00000372295.1:n.-31C>G | |
| ENST00000382848.5:c.-22-9C>G MANE Select | ENSP00000372299.4:n.-22-9C>G | |
| ENST00000382844.1:c.-31C>G | ENSP00000372295.1:n.-31C>G | |
| ENST00000382848.4:c.-22-9C>G | ENSP00000372299.4:n.-22-9C>G | |
| NM_004004.5:c.-22-9C>G | NP_003995.2:n.-22-9C>G | |
| XM_011535049.1:c.-22-9C>G | XP_011533351.1:n.-22-9C>G | |
| XM_011535049.2:c.-22-9C>G | XP_011533351.1:n.-22-9C>G | |
| NM_004004.6:c.-22-9C>G MANE Select | NP_003995.2:n.-22-9C>G |