Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52814109C>T , CM000674.2:g.52814109C>T | GRCh38 |
| NC_000012.11:g.53207893C>T , CM000674.1:g.53207893C>T | GRCh37 |
| NC_000012.10:g.51494160C>T | NCBI36 |
| NG_007380.1:g.5443G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551956.2:c.-51G>A MANE Select | ENSP00000448220.1:n.-51G>A | |
| ENST00000548097.5:c.-51G>A | ENSP00000449755.1:n.-51G>A | |
| ENST00000551956.1:c.-51G>A | ENSP00000448220.1:n.-51G>A | |
| ENST00000552668.1:c.-51G>A | ENSP00000447320.1:n.-51G>A | |
| NM_002272.3:c.-51G>A | NP_002263.3:n.-51G>A | |
| NM_002272.4:c.-51G>A MANE Select | NP_002263.3:n.-51G>A |