Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.228174726C>T , CM000663.2:g.228174726C>T | GRCh38 |
| NC_000001.10:g.228362427C>T , CM000663.1:g.228362427C>T | GRCh37 |
| NC_000001.9:g.226429050C>T | NCBI36 |
| NG_042231.1:g.13919C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001010867.4:c.376C>T MANE Select | NP_001010867.1:p.Leu126= |
| ENST00000366711.4:c.376C>T MANE Select | ENSP00000355672.3:p.Leu126= |
| NM_001010867.2:c.376C>T | NP_001010867.1:p.Leu126= |
| NM_001010867.3:c.376C>T | NP_001010867.1:p.Leu126= |
| NM_001310327.1:c.-204C>T | NP_001297256.1:n.-204C>T |
| NM_001310327.2:c.-204C>T | NP_001297256.1:n.-204C>T |
| ENST00000366711.3:c.376C>T | ENSP00000355672.3:p.Leu126= |
| ENST00000484749.5:n.2376C>T | |
| ENST00000546123.2:n.96C>T | |
| XM_006711753.2:c.376C>T | XP_006711816.1:p.Leu126= |