Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213477C>A , CM000667.2:g.1213477C>A | GRCh38 |
| NC_000005.9:g.1213592C>A , CM000667.1:g.1213592C>A | GRCh37 |
| NC_000005.8:g.1266592C>A | NCBI36 |
| NG_008282.1:g.16883C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.678C>A MANE Select | ENSP00000305302.10:p.Thr226= | |
| ENST00000304460.10:c.678C>A | ENSP00000305302.10:p.Thr226= | |
| ENST00000515652.5:c.586C>A | ENSP00000425701.1:p.Leu196Ile | |
| NM_001003841.2:c.678C>A | NP_001003841.1:p.Thr226= | |
| NM_001003841.3:c.678C>A MANE Select | NP_001003841.1:p.Thr226= |