HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44374708G>T , CM000679.2:g.44374708G>T | GRCh38 |
NC_000017.10:g.42452076G>T , CM000679.1:g.42452076G>T | GRCh37 |
NC_000017.9:g.39807602G>T | NCBI36 |
NG_008331.1:g.19798C>A , LRG_479:g.19798C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262407.6:c.2894C>A MANE Select | ENSP00000262407.5:p.Ser965Tyr | |
ENST00000648408.1:c.2325C>A | ||
ENST00000262407.5:c.2894C>A | ENSP00000262407.5:p.Ser965Tyr | |
ENST00000587295.5:c.253+1125C>A | ||
ENST00000592462.5:n.2405C>A | ||
NM_000419.3:c.2894C>A , LRG_479t1:c.2894C>A | NP_000410.2:p.Ser965Tyr | |
XM_011524749.1:c.2842-238C>A | XP_011523051.1:n.2842-238C>A | |
XM_011524750.1:c.2894C>A | XP_011523052.1:p.Ser965Tyr | |
NM_000419.4:c.2894C>A | NP_000410.2:p.Ser965Tyr | |
NM_000419.5:c.2894C>A MANE Select | NP_000410.2:p.Ser965Tyr |