Canonical Allele Identifier: CA382077901
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.89017982A>C (hg19) chr11:g.89284814A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89284814A>C , CM000673.2:g.89284814A>C GRCh38
NC_000011.9:g.89017982A>C , CM000673.1:g.89017982A>C GRCh37
NC_000011.8:g.88657630A>C NCBI36
NG_008748.1:g.111943A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.1226A>C MANE Select ENSP00000263321.4:p.Glu409Ala
ENST00000263321.5:c.1226A>C ENSP00000263321.4:p.Glu409Ala
ENST00000528243.1:n.224A>C
NM_000372.4:c.1226A>C NP_000363.1:p.Glu409Ala
XM_011542970.1:c.1226A>C XP_011541272.1:p.Glu409Ala
XM_011542970.2:c.1226A>C XP_011541272.1:p.Glu409Ala
XR_001748321.1:n.2456+1220T>G
XR_001748322.1:n.2457+1220T>G
NM_000372.5:c.1226A>C MANE Select NP_000363.1:p.Glu409Ala
Search 100 bp 5'
Search 100 bp 3'