HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44372416A>T , CM000679.2:g.44372416A>T | GRCh38 |
NC_000017.10:g.42449784A>T , CM000679.1:g.42449784A>T | GRCh37 |
NC_000017.9:g.39805310A>T | NCBI36 |
NG_008331.1:g.22090T>A , LRG_479:g.22090T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262407.6:c.3068T>A MANE Select | ENSP00000262407.5:p.Phe1023Tyr | |
ENST00000648408.1:c.2382T>A | ||
ENST00000262407.5:c.3068T>A | ENSP00000262407.5:p.Phe1023Tyr | |
ENST00000587295.5:c.261T>A | ||
ENST00000588098.1:c.45T>A | ||
NM_000419.3:c.3068T>A , LRG_479t1:c.3068T>A | NP_000410.2:p.Phe1023Tyr | |
XM_011524749.1:c.2966T>A | XP_011523051.1:p.Phe989Tyr | |
XM_011524750.1:c.2951T>A | XP_011523052.1:p.Phe984Tyr | |
NM_000419.4:c.3068T>A | NP_000410.2:p.Phe1023Tyr | |
NM_000419.5:c.3068T>A MANE Select | NP_000410.2:p.Phe1023Tyr |