HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583884A>G , CM000679.2:g.41583884A>G | GRCh38 |
NC_000017.10:g.39740136A>G , CM000679.1:g.39740136A>G | GRCh37 |
NC_000017.9:g.36993662A>G | NCBI36 |
NG_008624.1:g.8012T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.803T>C MANE Select | ENSP00000167586.6:p.Val268Ala | |
ENST00000167586.6:c.803T>C | ENSP00000167586.6:p.Val268Ala | |
ENST00000476662.1:n.253T>C | ||
NM_000526.4:c.803T>C | NP_000517.2:p.Val268Ala | |
NM_000526.5:c.803T>C MANE Select | NP_000517.3:p.Val268Ala |