Canonical Allele Identifier: CA2574945831

Gene: TYR

Linked Data

• gnomAD v4: 11-89284707-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284707A>G , CM000673.2:g.89284707A>G	GRCh38
NC_000011.9:g.89017875A>G , CM000673.1:g.89017875A>G	GRCh37
NC_000011.8:g.88657523A>G	NCBI36
NG_008748.1:g.111836A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.1185-66A>G MANE Select	ENSP00000263321.4:n.1185-66A>G
ENST00000263321.5:c.1185-66A>G	ENSP00000263321.4:n.1185-66A>G
ENST00000528243.1:n.183-66A>G
NM_000372.4:c.1185-66A>G	NP_000363.1:n.1185-66A>G
XM_011542970.1:c.1185-66A>G	XP_011541272.1:n.1185-66A>G
XM_011542970.2:c.1185-66A>G	XP_011541272.1:n.1185-66A>G
XR_001748321.1:n.2456+1327T>C
XR_001748322.1:n.2457+1327T>C
NM_000372.5:c.1185-66A>G MANE Select	NP_000363.1:n.1185-66A>G