Linked Data
dbSNP Id:
rs779122055
ExAC:
4:73179377 T / A
gnomAD v2:
4-73179377-T-A
gnomAD v4:
4-72313660-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.72313660T>A , CM000666.2:g.72313660T>A | GRCh38 |
| NC_000004.11:g.73179377T>A , CM000666.1:g.73179377T>A | GRCh37 |
| NC_000004.10:g.73398241T>A | NCBI36 |
| NG_046955.1:g.260140A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286657.10:c.1745+17A>T MANE Select | ENSP00000286657.4:n.1745+17A>T | |
| ENST00000286657.8:c.1745+17A>T | ENSP00000286657.4:n.1745+17A>T | |
| ENST00000622135.1:c.1745+17A>T | ENSP00000480055.1:n.1745+17A>T | |
| NM_014243.2:c.1745+17A>T | NP_055058.2:n.1745+17A>T | |
| XM_011532421.1:c.1688+17A>T | XP_011530723.1:n.1688+17A>T | |
| XM_011532422.1:c.1661+17A>T | XP_011530724.1:n.1661+17A>T | |
| XM_011532423.1:c.1103+17A>T | XP_011530725.1:n.1103+17A>T | |
| XM_011532424.1:c.1013+17A>T | XP_011530726.1:n.1013+17A>T | |
| XM_011532421.2:c.1688+17A>T | XP_011530723.1:n.1688+17A>T | |
| XM_011532422.3:c.1661+17A>T | XP_011530724.1:n.1661+17A>T | |
| NM_014243.3:c.1745+17A>T MANE Select | NP_055058.2:n.1745+17A>T |