Canonical Allele Identifier: CA476159001

Gene: TYR

Linked Data

• dbSNP Id: rs1943261339
• gnomAD v4: 11-89178664-C-T
• MyVariant Identifiers: chr11:g.88911832C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178664C>T , CM000673.2:g.89178664C>T	GRCh38
NC_000011.9:g.88911832C>T , CM000673.1:g.88911832C>T	GRCh37
NC_000011.8:g.88551480C>T	NCBI36
NG_008748.1:g.5793C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.711C>T MANE Select	ENSP00000263321.4:p.Asp237=
ENST00000263321.5:c.711C>T	ENSP00000263321.4:p.Asp237=
ENST00000526139.1:n.772C>T
NM_000372.4:c.711C>T	NP_000363.1:p.Asp237=
XM_011542970.1:c.711C>T	XP_011541272.1:p.Asp237=
XM_011542970.2:c.711C>T	XP_011541272.1:p.Asp237=
XR_001748321.1:n.2718-65131G>A
XR_001748322.1:n.2733-65131G>A
NM_000372.5:c.711C>T MANE Select	NP_000363.1:p.Asp237=