Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992623A>T , CM000670.2:g.16992623A>T | GRCh38 |
| NC_000008.10:g.16850132A>T , CM000670.1:g.16850132A>T | GRCh37 |
| NC_000008.9:g.16894503A>T | NCBI36 |
| NG_015978.1:g.14543T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019851.3:c.*449T>A MANE Select | NP_062825.1:n.*449T>A |
| ENST00000180166.6:c.*449T>A MANE Select | ENSP00000180166.5:n.*449T>A |
| ENST00000180166.5:c.*449T>A | ENSP00000180166.5:n.*449T>A |