Canonical Allele Identifier: CA1989921881

Gene: TYR

Linked Data

• dbSNP Id: rs1591134822
• gnomAD v4: 11-89178918-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178918T>G , CM000673.2:g.89178918T>G	GRCh38
NC_000011.9:g.88912086T>G , CM000673.1:g.88912086T>G	GRCh37
NC_000011.8:g.88551734T>G	NCBI36
NG_008748.1:g.6047T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+146T>G MANE Select	ENSP00000263321.4:n.819+146T>G
ENST00000263321.5:c.819+146T>G	ENSP00000263321.4:n.819+146T>G
ENST00000526139.1:n.880+146T>G
NM_000372.4:c.819+146T>G	NP_000363.1:n.819+146T>G
XM_011542970.1:c.819+146T>G	XP_011541272.1:n.819+146T>G
XM_011542970.2:c.819+146T>G	XP_011541272.1:n.819+146T>G
XR_001748321.1:n.2718-65385A>C
XR_001748322.1:n.2733-65385A>C
NM_000372.5:c.819+146T>G MANE Select	NP_000363.1:n.819+146T>G