Linked Data
gnomAD v4:
3-50345765-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.50345765C>T , CM000665.2:g.50345765C>T | GRCh38 |
| NC_000003.11:g.50383196C>T , CM000665.1:g.50383196C>T | GRCh37 |
| NC_000003.10:g.50358200C>T | NCBI36 |
| NG_023270.1:g.172G>A | |
| NG_042828.1:g.4982G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000231749.7:c.-186G>A | ENSP00000231749.3:n.-186G>A | |
| XM_005265216.2:c.-314G>A | XP_005265273.1:n.-314G>A |