Canonical Allele Identifier: CA476157166
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs61753184
MyVariant Identifiers: chr11:g.88911350C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178182C>A , CM000673.2:g.89178182C>A GRCh38
NC_000011.9:g.88911350C>A , CM000673.1:g.88911350C>A GRCh37
NC_000011.8:g.88550998C>A NCBI36
NG_008748.1:g.5311C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.229C>A MANE Select ENSP00000263321.4:p.Arg77=
ENST00000263321.5:c.229C>A ENSP00000263321.4:p.Arg77=
ENST00000526139.1:n.290C>A
NM_000372.4:c.229C>A NP_000363.1:p.Arg77=
XM_011542970.1:c.229C>A XP_011541272.1:p.Arg77=
XM_011542970.2:c.229C>A XP_011541272.1:p.Arg77=
XR_001748321.1:n.2718-64649G>T
XR_001748322.1:n.2733-64649G>T
NM_000372.5:c.229C>A MANE Select NP_000363.1:p.Arg77=
Search 100 bp 5'
Search 100 bp 3'