Canonical Allele Identifier: CA1989938094

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89191286G= , CM000673.2:g.89191286G=	GRCh38
NC_000011.9:g.88924454G= , CM000673.1:g.88924454G=	GRCh37
NC_000011.8:g.88564102G=	NCBI36
NG_008748.1:g.18415G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.904G= MANE Select	ENSP00000263321.4:p.Gly302=
ENST00000263321.5:c.904G=	ENSP00000263321.4:p.Gly302=
ENST00000526139.1:n.965G=
NM_000372.4:c.904G=	NP_000363.1:p.Gly302=
XM_011542970.1:c.904G=	XP_011541272.1:p.Gly302=
XM_011542970.2:c.904G=	XP_011541272.1:p.Gly302=
XR_001748321.1:n.2718-77753C=
XR_001748322.1:n.2733-77753C=
NM_000372.5:c.904G= MANE Select	NP_000363.1:p.Gly302=