Canonical Allele Identifier: CA2615470699

Gene: TYR

Linked Data

• gnomAD v4: 11-89178882-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178882G>T , CM000673.2:g.89178882G>T	GRCh38
NC_000011.9:g.88912050G>T , CM000673.1:g.88912050G>T	GRCh37
NC_000011.8:g.88551698G>T	NCBI36
NG_008748.1:g.6011G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+110G>T MANE Select	ENSP00000263321.4:n.819+110G>T
ENST00000263321.5:c.819+110G>T	ENSP00000263321.4:n.819+110G>T
ENST00000526139.1:n.880+110G>T
NM_000372.4:c.819+110G>T	NP_000363.1:n.819+110G>T
XM_011542970.1:c.819+110G>T	XP_011541272.1:n.819+110G>T
XM_011542970.2:c.819+110G>T	XP_011541272.1:n.819+110G>T
XR_001748321.1:n.2718-65349C>A
XR_001748322.1:n.2733-65349C>A
NM_000372.5:c.819+110G>T MANE Select	NP_000363.1:n.819+110G>T