Canonical Allele Identifier: CA382034325
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs1400722833
gnomAD v2: 11-88911523-T-A
gnomAD v3: 11-89178355-T-A
gnomAD v4: 11-89178355-T-A
MyVariant Identifiers: chr11:g.88911523T>A (hg19) chr11:g.89178355T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178355T>A , CM000673.2:g.89178355T>A GRCh38
NC_000011.9:g.88911523T>A , CM000673.1:g.88911523T>A GRCh37
NC_000011.8:g.88551171T>A NCBI36
NG_008748.1:g.5484T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.402T>A MANE Select ENSP00000263321.4:p.Phe134Leu
ENST00000263321.5:c.402T>A ENSP00000263321.4:p.Phe134Leu
ENST00000526139.1:n.463T>A
NM_000372.4:c.402T>A NP_000363.1:p.Phe134Leu
XM_011542970.1:c.402T>A XP_011541272.1:p.Phe134Leu
XM_011542970.2:c.402T>A XP_011541272.1:p.Phe134Leu
XR_001748321.1:n.2718-64822A>T
XR_001748322.1:n.2733-64822A>T
NM_000372.5:c.402T>A MANE Select NP_000363.1:p.Phe134Leu
Search 100 bp 5'
Search 100 bp 3'