Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19704954T>A , CM000686.2:g.19704954T>A | GRCh38 |
| NC_000024.9:g.21866840T>A , CM000686.1:g.21866840T>A | GRCh37 |
| NC_000024.8:g.20326228T>A | NCBI36 |
| NG_032920.1:g.44986A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000317961.9:c.*1041A>T MANE Select | ENSP00000322408.4:n.*1041A>T | |
| ENST00000469599.6:n.4412A>T | ||
| NM_001146706.2:c.*1041A>T | NP_001140178.1:n.*1041A>T | |
| NM_004653.5:c.*1041A>T MANE Select | NP_004644.2:n.*1041A>T | |
| NM_001146705.2:c.*1041A>T | NP_001140177.1:n.*1041A>T |