Canonical Allele Identifier: CA681530191

Gene: TYR

Linked Data

• dbSNP Id: rs1382876668
• gnomAD v4: 11-89284729-A-G
• MyVariant Identifiers: chr11:g.89017897A>G (hg19) ; chr11:g.89284729A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284729A>G , CM000673.2:g.89284729A>G	GRCh38
NC_000011.9:g.89017897A>G , CM000673.1:g.89017897A>G	GRCh37
NC_000011.8:g.88657545A>G	NCBI36
NG_008748.1:g.111858A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.1185-44A>G MANE Select	ENSP00000263321.4:n.1185-44A>G
ENST00000263321.5:c.1185-44A>G	ENSP00000263321.4:n.1185-44A>G
ENST00000528243.1:n.183-44A>G
NM_000372.4:c.1185-44A>G	NP_000363.1:n.1185-44A>G
XM_011542970.1:c.1185-44A>G	XP_011541272.1:n.1185-44A>G
XM_011542970.2:c.1185-44A>G	XP_011541272.1:n.1185-44A>G
XR_001748321.1:n.2456+1305T>C
XR_001748322.1:n.2457+1305T>C
NM_000372.5:c.1185-44A>G MANE Select	NP_000363.1:n.1185-44A>G