Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232543658C>T , CM000664.2:g.232543658C>T | GRCh38 |
| NC_000002.11:g.233408368C>T , CM000664.1:g.233408368C>T | GRCh37 |
| NC_000002.10:g.233116612C>T | NCBI36 |
| NG_012954.1:g.8932C>T | |
| NG_012954.2:g.8967C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005199.5:c.994C>T MANE Select | NP_005190.4:p.Arg332Trp |
| ENST00000651502.1:c.994C>T MANE Select | ENSP00000498757.1:p.Arg332Trp |
| NM_005199.4:c.994C>T | NP_005190.4:p.Arg332Trp |
| ENST00000389492.3:c.838C>T | ENSP00000374143.3:p.Arg280Trp |
| ENST00000389494.7:c.994C>T | ENSP00000374145.3:p.Arg332Trp |