Linked Data
dbSNP Id:
rs751438870
ExAC:
1:1447723 G / T
gnomAD v2:
1-1447723-G-T
gnomAD v3:
1-1512343-G-T
gnomAD v4:
1-1512343-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1512343G>T , CM000663.2:g.1512343G>T | GRCh38 |
| NC_000001.10:g.1447723G>T , CM000663.1:g.1447723G>T | GRCh37 |
| NC_000001.9:g.1437586G>T | NCBI36 |
| NG_053035.1:g.5201G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378756.8:c.75G>T MANE Select | ENSP00000368031.3:p.Ala25= | |
| ENST00000672388.1:n.179G>T | ||
| ENST00000378755.9:c.75G>T | ENSP00000368030.5:p.Ala25= | |
| ENST00000378756.7:c.75G>T | ENSP00000368031.3:p.Ala25= | |
| NM_001170535.1:c.75G>T | NP_001164006.1:p.Ala25= | |
| NM_018188.3:c.75G>T | NP_060658.3:p.Ala25= | |
| NM_001170535.2:c.75G>T | NP_001164006.1:p.Ala25= | |
| NM_018188.4:c.75G>T | NP_060658.3:p.Ala25= | |
| XM_024448098.1:c.75G>T | XP_024303866.1:p.Ala25= | |
| XR_001737282.1:n.201G>T | ||
| XR_002956997.1:n.201G>T | ||
| NM_001170535.3:c.75G>T MANE Select | NP_001164006.1:p.Ala25= | |
| NM_018188.5:c.75G>T | NP_060658.3:p.Ala25= |