HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322924C>A , CM000677.2:g.73322924C>A | GRCh38 |
NC_000015.9:g.73615265C>A , CM000677.1:g.73615265C>A | GRCh37 |
NC_000015.8:g.71402318C>A | NCBI36 |
NG_009063.1:g.51341G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3169G>T MANE Select | ENSP00000261917.3:p.Ala1057Ser | |
ENST00000261917.3:c.3169G>T | ENSP00000261917.3:p.Ala1057Ser | |
NM_005477.2:c.3169G>T | NP_005468.1:p.Ala1057Ser | |
XM_011521148.1:c.1951G>T | XP_011519450.1:p.Ala651Ser | |
XM_011521148.2:c.1951G>T | XP_011519450.1:p.Ala651Ser | |
NM_005477.3:c.3169G>T MANE Select | NP_005468.1:p.Ala1057Ser |