HGVS | Genome Assembly |
---|---|
NC_000020.11:g.57562855T>A , CM000682.2:g.57562855T>A | GRCh38 |
NC_000020.10:g.56137911T>A , CM000682.1:g.56137911T>A | GRCh37 |
NC_000020.9:g.55571317T>A | NCBI36 |
NG_008205.1:g.6775T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319441.6:c.566T>A MANE Select | ENSP00000319814.4:p.Phe189Tyr | |
ENST00000319441.5:c.566T>A | ENSP00000319814.4:p.Phe189Tyr | |
ENST00000467047.1:n.1776T>A | ||
ENST00000470051.1:n.22T>A | ||
ENST00000498194.1:n.508T>A | ||
NM_002591.3:c.566T>A | NP_002582.3:p.Phe189Tyr | |
XM_011528839.1:c.170T>A | XP_011527141.1:p.Phe57Tyr | |
XM_024451888.1:c.170T>A | XP_024307656.1:p.Phe57Tyr | |
NM_002591.4:c.566T>A MANE Select | NP_002582.3:p.Phe189Tyr |