Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101421370A>G , CM000671.2:g.101421370A>G | GRCh38 |
| NC_000009.11:g.104183652A>G , CM000671.1:g.104183652A>G | GRCh37 |
| NC_000009.10:g.103223473A>G | NCBI36 |
| NG_012387.1:g.19411T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.*439T>C MANE Select | ENSP00000497767.1:n.*439T>C | |
| ENST00000374855.8:c.*439T>C | ENSP00000363988.4:n.*439T>C | |
| NM_000035.3:c.*439T>C | NP_000026.2:n.*439T>C | |
| NM_000035.4:c.*439T>C MANE Select | NP_000026.2:n.*439T>C |