Canonical Allele Identifier: CA382033849
Gene: TYR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178188T>A , CM000673.2:g.89178188T>A GRCh38
NC_000011.9:g.88911356T>A , CM000673.1:g.88911356T>A GRCh37
NC_000011.8:g.88551004T>A NCBI36
NG_008748.1:g.5317T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.235T>A MANE Select ENSP00000263321.4:p.Ser79Thr
ENST00000263321.5:c.235T>A ENSP00000263321.4:p.Ser79Thr
ENST00000526139.1:n.296T>A
NM_000372.4:c.235T>A NP_000363.1:p.Ser79Thr
XM_011542970.1:c.235T>A XP_011541272.1:p.Ser79Thr
XM_011542970.2:c.235T>A XP_011541272.1:p.Ser79Thr
XR_001748321.1:n.2718-64655A>T
XR_001748322.1:n.2733-64655A>T
NM_000372.5:c.235T>A MANE Select NP_000363.1:p.Ser79Thr