Canonical Allele Identifier: CA476159118
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.88911859T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178691T>C , CM000673.2:g.89178691T>C GRCh38
NC_000011.9:g.88911859T>C , CM000673.1:g.88911859T>C GRCh37
NC_000011.8:g.88551507T>C NCBI36
NG_008748.1:g.5820T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.738T>C MANE Select ENSP00000263321.4:p.Ile246=
ENST00000263321.5:c.738T>C ENSP00000263321.4:p.Ile246=
ENST00000526139.1:n.799T>C
NM_000372.4:c.738T>C NP_000363.1:p.Ile246=
XM_011542970.1:c.738T>C XP_011541272.1:p.Ile246=
XM_011542970.2:c.738T>C XP_011541272.1:p.Ile246=
XR_001748321.1:n.2718-65158A>G
XR_001748322.1:n.2733-65158A>G
NM_000372.5:c.738T>C MANE Select NP_000363.1:p.Ile246=
Search 100 bp 5'
Search 100 bp 3'