Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536391T>G , CM000679.2:g.42536391T>G | GRCh38 |
| NC_000017.10:g.40688409T>G , CM000679.1:g.40688409T>G | GRCh37 |
| NC_000017.9:g.37941935T>G | NCBI36 |
| NG_011552.1:g.5459T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.119T>G MANE Select | ENSP00000225927.1:p.Leu40Arg | |
| ENST00000225927.6:c.119T>G | ENSP00000225927.1:p.Leu40Arg | |
| NM_000263.3:c.119T>G | NP_000254.2:p.Leu40Arg | |
| XM_024450771.1:c.119T>G | XP_024306539.1:p.Leu40Arg | |
| NM_000263.4:c.119T>G MANE Select | NP_000254.2:p.Leu40Arg |