Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.90915854C>T , CM000672.2:g.90915854C>T | GRCh38 |
| NC_000010.10:g.92675611C>T , CM000672.1:g.92675611C>T | GRCh37 |
| NC_000010.9:g.92665591C>T | NCBI36 |
| NG_023227.1:g.10422G>A , LRG_379:g.10422G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371697.4:c.678G>A MANE Select | ENSP00000360762.3:p.Ala226= | |
| ENST00000371697.3:c.678G>A | ENSP00000360762.3:p.Ala226= | |
| NM_014391.2:c.678G>A , LRG_379t1:c.678G>A | NP_055206.2:p.Ala226= | |
| NM_014391.3:c.678G>A MANE Select | NP_055206.2:p.Ala226= |