Linked Data
gnomAD v4:
3-165069031-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165069031C>A , CM000665.2:g.165069031C>A | GRCh38 |
| NC_000003.11:g.164786819C>A , CM000665.1:g.164786819C>A | GRCh37 |
| NC_000003.10:g.166269513C>A | NCBI36 |
| NG_017043.1:g.14465G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264382.8:c.373+47G>T MANE Select | ENSP00000264382.3:n.373+47G>T | |
| ENST00000264382.7:c.373+47G>T | ENSP00000264382.3:n.373+47G>T | |
| ENST00000476593.1:c.*248+47G>T | ENSP00000419450.1:n.*248+47G>T | |
| NM_001041.3:c.373+47G>T | NP_001032.2:n.373+47G>T | |
| XM_011513078.1:c.274+47G>T | XP_011511380.1:n.274+47G>T | |
| XM_011513078.2:c.274+47G>T | XP_011511380.1:n.274+47G>T | |
| NM_001041.4:c.373+47G>T MANE Select | NP_001032.2:n.373+47G>T |