Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135028911G>A , CM000667.2:g.135028911G>A | GRCh38 |
| NC_000005.9:g.134364601G>A , CM000667.1:g.134364601G>A | GRCh37 |
| NC_000005.8:g.134392500G>A | NCBI36 |
| NG_012114.1:g.10364C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.813C>T MANE Select | ENSP00000265340.6:p.Tyr271= | |
| ENST00000265340.11:c.813C>T | ENSP00000265340.6:p.Tyr271= | |
| ENST00000506438.5:c.813C>T | ENSP00000427542.1:p.Tyr271= | |
| NM_002653.4:c.813C>T | NP_002644.4:p.Tyr271= | |
| NM_002653.5:c.813C>T MANE Select | NP_002644.4:p.Tyr271= |