Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.228166155C>T , CM000663.2:g.228166155C>T | GRCh38 |
| NC_000001.10:g.228353856C>T , CM000663.1:g.228353856C>T | GRCh37 |
| NC_000001.9:g.226420479C>T | NCBI36 |
| NG_042231.1:g.5348C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001010867.4:c.339C>T MANE Select | NP_001010867.1:p.Tyr113= |
| ENST00000366711.4:c.339C>T MANE Select | ENSP00000355672.3:p.Tyr113= |
| NM_001010867.2:c.339C>T | NP_001010867.1:p.Tyr113= |
| NM_001010867.3:c.339C>T | NP_001010867.1:p.Tyr113= |
| ENST00000366711.3:c.339C>T | ENSP00000355672.3:p.Tyr113= |
| XM_006711753.2:c.339C>T | XP_006711816.1:p.Tyr113= |