Canonical Allele Identifier: CA382034718
Gene: TYR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178522G>T , CM000673.2:g.89178522G>T GRCh38
NC_000011.9:g.88911690G>T , CM000673.1:g.88911690G>T GRCh37
NC_000011.8:g.88551338G>T NCBI36
NG_008748.1:g.5651G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.569G>T MANE Select ENSP00000263321.4:p.Gly190Val
ENST00000263321.5:c.569G>T ENSP00000263321.4:p.Gly190Val
ENST00000526139.1:n.630G>T
NM_000372.4:c.569G>T NP_000363.1:p.Gly190Val
XM_011542970.1:c.569G>T XP_011541272.1:p.Gly190Val
XM_011542970.2:c.569G>T XP_011541272.1:p.Gly190Val
XR_001748321.1:n.2718-64989C>A
XR_001748322.1:n.2733-64989C>A
NM_000372.5:c.569G>T MANE Select NP_000363.1:p.Gly190Val