Canonical Allele Identifier: CA382035844

Gene: TYR

Linked Data

• dbSNP Id: rs1943441434
• MyVariant Identifiers: chr11:g.88924454G>T (hg19) ; chr11:g.89191286G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.904G>T MANE Select	ENSP00000263321.4:p.Gly302Ter
ENST00000263321.5:c.904G>T	ENSP00000263321.4:p.Gly302Ter
ENST00000526139.1:n.965G>T
NM_000372.4:c.904G>T	NP_000363.1:p.Gly302Ter
XM_011542970.1:c.904G>T	XP_011541272.1:p.Gly302Ter
XM_011542970.2:c.904G>T	XP_011541272.1:p.Gly302Ter
XR_001748321.1:n.2718-77753C>A
XR_001748322.1:n.2733-77753C>A
NM_000372.5:c.904G>T MANE Select	NP_000363.1:p.Gly302Ter