Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.50345805A>T , CM000665.2:g.50345805A>T | GRCh38 |
| NC_000003.11:g.50383236A>T , CM000665.1:g.50383236A>T | GRCh37 |
| NC_000003.10:g.50358240A>T | NCBI36 |
| NG_023270.1:g.132T>A | |
| NG_042828.1:g.4942T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000231749.7:c.-226T>A | ENSP00000231749.3:n.-226T>A | |
| XM_005265216.2:c.-354T>A | XP_005265273.1:n.-354T>A |