Canonical Allele Identifier: CA476158973
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.88924456A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89191288A>C , CM000673.2:g.89191288A>C GRCh38
NC_000011.9:g.88924456A>C , CM000673.1:g.88924456A>C GRCh37
NC_000011.8:g.88564104A>C NCBI36
NG_008748.1:g.18417A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.906A>C MANE Select ENSP00000263321.4:p.Gly302=
ENST00000263321.5:c.906A>C ENSP00000263321.4:p.Gly302=
ENST00000526139.1:n.967A>C
NM_000372.4:c.906A>C NP_000363.1:p.Gly302=
XM_011542970.1:c.906A>C XP_011541272.1:p.Gly302=
XM_011542970.2:c.906A>C XP_011541272.1:p.Gly302=
XR_001748321.1:n.2718-77755T>G
XR_001748322.1:n.2733-77755T>G
NM_000372.5:c.906A>C MANE Select NP_000363.1:p.Gly302=
Search 100 bp 5'
Search 100 bp 3'