Canonical Allele Identifier: CA476157172

Gene: TYR

Linked Data

• MyVariant Identifiers: chr11:g.88911358G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178190G>T , CM000673.2:g.89178190G>T	GRCh38
NC_000011.9:g.88911358G>T , CM000673.1:g.88911358G>T	GRCh37
NC_000011.8:g.88551006G>T	NCBI36
NG_008748.1:g.5319G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.237G>T MANE Select	ENSP00000263321.4:p.Ser79=
ENST00000263321.5:c.237G>T	ENSP00000263321.4:p.Ser79=
ENST00000526139.1:n.298G>T
NM_000372.4:c.237G>T	NP_000363.1:p.Ser79=
XM_011542970.1:c.237G>T	XP_011541272.1:p.Ser79=
XM_011542970.2:c.237G>T	XP_011541272.1:p.Ser79=
XR_001748321.1:n.2718-64657C>A
XR_001748322.1:n.2733-64657C>A
NM_000372.5:c.237G>T MANE Select	NP_000363.1:p.Ser79=