HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44296384A= , CM000683.2:g.44296384A= | GRCh38 |
NC_000021.8:g.45716267A= , CM000683.1:g.45716267A= | GRCh37 |
NC_000021.7:g.44540695A= | NCBI36 |
NG_009556.1:g.15505A= , LRG_18:g.15505A= | |
NG_034033.1:g.1351A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.1505A= MANE Select | ENSP00000291582.5:p.Asp502= | |
ENST00000291582.5:c.1505A= | ENSP00000291582.5:p.Asp502= | |
ENST00000337909.5:n.966A= | ||
ENST00000397994.8:n.884A= | ||
ENST00000527919.5:n.2264A= | ||
ENST00000530812.5:n.3252A= | ||
NM_000383.3:c.1505A= | NP_000374.1:p.Asp502= | |
XM_011529551.1:c.1502A= | XP_011527853.1:p.Asp501= | |
NM_000383.4:c.1505A= MANE Select | NP_000374.1:p.Asp502= |