Canonical Allele Identifier: CA2574945798

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178869A>G , CM000673.2:g.89178869A>G	GRCh38
NC_000011.9:g.88912037A>G , CM000673.1:g.88912037A>G	GRCh37
NC_000011.8:g.88551685A>G	NCBI36
NG_008748.1:g.5998A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+97A>G MANE Select	ENSP00000263321.4:n.819+97A>G
ENST00000263321.5:c.819+97A>G	ENSP00000263321.4:n.819+97A>G
ENST00000526139.1:n.880+97A>G
NM_000372.4:c.819+97A>G	NP_000363.1:n.819+97A>G
XM_011542970.1:c.819+97A>G	XP_011541272.1:n.819+97A>G
XM_011542970.2:c.819+97A>G	XP_011541272.1:n.819+97A>G
XR_001748321.1:n.2718-65336T>C
XR_001748322.1:n.2733-65336T>C
NM_000372.5:c.819+97A>G MANE Select	NP_000363.1:n.819+97A>G