Canonical Allele Identifier: CA476159021
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.88911838G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178670G>A , CM000673.2:g.89178670G>A GRCh38
NC_000011.9:g.88911838G>A , CM000673.1:g.88911838G>A GRCh37
NC_000011.8:g.88551486G>A NCBI36
NG_008748.1:g.5799G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.717G>A MANE Select ENSP00000263321.4:p.Arg239=
ENST00000263321.5:c.717G>A ENSP00000263321.4:p.Arg239=
ENST00000526139.1:n.778G>A
NM_000372.4:c.717G>A NP_000363.1:p.Arg239=
XM_011542970.1:c.717G>A XP_011541272.1:p.Arg239=
XM_011542970.2:c.717G>A XP_011541272.1:p.Arg239=
XR_001748321.1:n.2718-65137C>T
XR_001748322.1:n.2733-65137C>T
NM_000372.5:c.717G>A MANE Select NP_000363.1:p.Arg239=
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