HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73323053C>T , CM000677.2:g.73323053C>T | GRCh38 |
NC_000015.9:g.73615394C>T , CM000677.1:g.73615394C>T | GRCh37 |
NC_000015.8:g.71402447C>T | NCBI36 |
NG_009063.1:g.51212G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3040G>A MANE Select | ENSP00000261917.3:p.Ala1014Thr | |
ENST00000261917.3:c.3040G>A | ENSP00000261917.3:p.Ala1014Thr | |
NM_005477.2:c.3040G>A | NP_005468.1:p.Ala1014Thr | |
XM_011521148.1:c.1822G>A | XP_011519450.1:p.Ala608Thr | |
XM_011521148.2:c.1822G>A | XP_011519450.1:p.Ala608Thr | |
NM_005477.3:c.3040G>A MANE Select | NP_005468.1:p.Ala1014Thr |