Canonical Allele Identifier: CA6221076
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs13312740
ExAC: 11:88911390 A / G
gnomAD v2: 11-88911390-A-G
gnomAD v4: 11-89178222-A-G
MyVariant Identifiers: chr11:g.88911390A>G (hg19) chr11:g.89178222A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178222A>G , CM000673.2:g.89178222A>G GRCh38
NC_000011.9:g.88911390A>G , CM000673.1:g.88911390A>G GRCh37
NC_000011.8:g.88551038A>G NCBI36
NG_008748.1:g.5351A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.269A>G MANE Select ENSP00000263321.4:p.Gln90Arg
ENST00000263321.5:c.269A>G ENSP00000263321.4:p.Gln90Arg
ENST00000526139.1:n.330A>G
NM_000372.4:c.269A>G NP_000363.1:p.Gln90Arg
XM_011542970.1:c.269A>G XP_011541272.1:p.Gln90Arg
XM_011542970.2:c.269A>G XP_011541272.1:p.Gln90Arg
XR_001748321.1:n.2718-64689T>C
XR_001748322.1:n.2733-64689T>C
NM_000372.5:c.269A>G MANE Select NP_000363.1:p.Gln90Arg
Search 100 bp 5'
Search 100 bp 3'