Canonical Allele Identifier: CA227556
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99560
ClinVar RCV Id: RCV000085943
dbSNP Id: rs61753252
gnomAD v2: 11-88911410-G-A
MyVariant Identifiers: chr11:g.88911410G>A (hg19) chr11:g.89178242G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178242G>A , CM000673.2:g.89178242G>A GRCh38
NC_000011.9:g.88911410G>A , CM000673.1:g.88911410G>A GRCh37
NC_000011.8:g.88551058G>A NCBI36
NG_008748.1:g.5371G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.289G>A MANE Select ENSP00000263321.4:p.Gly97Arg
ENST00000263321.5:c.289G>A ENSP00000263321.4:p.Gly97Arg
ENST00000526139.1:n.350G>A
NM_000372.4:c.289G>A NP_000363.1:p.Gly97Arg
XM_011542970.1:c.289G>A XP_011541272.1:p.Gly97Arg
XM_011542970.2:c.289G>A XP_011541272.1:p.Gly97Arg
XR_001748321.1:n.2718-64709C>T
XR_001748322.1:n.2733-64709C>T
NM_000372.5:c.289G>A MANE Select NP_000363.1:p.Gly97Arg
Search 100 bp 5'
Search 100 bp 3'