HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45804360A= , CM000681.2:g.45804360A= | GRCh38 |
NC_000019.9:g.46307618A= , CM000681.1:g.46307618A= | GRCh37 |
NC_000019.8:g.50999458A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221538.8:c.1545T= MANE Select | ENSP00000221538.2:p.Ala515= | |
ENST00000221538.7:c.1545T= | ENSP00000221538.2:p.Ala515= | |
ENST00000597055.1:c.1545T= | ENSP00000472630.1:p.Ala515= | |
ENST00000600188.5:c.753T= | ENSP00000471559.1:p.Ala251= | |
NM_030785.3:c.1545T= | NP_110412.1:p.Ala515= | |
XM_011527351.1:c.1545T= | XP_011525653.1:p.Ala515= | |
XM_011527351.2:c.1545T= | XP_011525653.1:p.Ala515= | |
NM_030785.4:c.1545T= MANE Select | NP_110412.1:p.Ala515= |