Canonical Allele Identifier: CA382034470
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.88911594A>C (hg19) chr11:g.89178426A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178426A>C , CM000673.2:g.89178426A>C GRCh38
NC_000011.9:g.88911594A>C , CM000673.1:g.88911594A>C GRCh37
NC_000011.8:g.88551242A>C NCBI36
NG_008748.1:g.5555A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.473A>C MANE Select ENSP00000263321.4:p.Gln158Pro
ENST00000263321.5:c.473A>C ENSP00000263321.4:p.Gln158Pro
ENST00000526139.1:n.534A>C
NM_000372.4:c.473A>C NP_000363.1:p.Gln158Pro
XM_011542970.1:c.473A>C XP_011541272.1:p.Gln158Pro
XM_011542970.2:c.473A>C XP_011541272.1:p.Gln158Pro
XR_001748321.1:n.2718-64893T>G
XR_001748322.1:n.2733-64893T>G
NM_000372.5:c.473A>C MANE Select NP_000363.1:p.Gln158Pro
Search 100 bp 5'
Search 100 bp 3'