Canonical Allele Identifier: CA382034138

Gene: TYR

Linked Data

• dbSNP Id: rs759163678
• gnomAD v4: 11-89178269-G-T
• MyVariant Identifiers: chr11:g.88911437G>T (hg19) ; chr11:g.89178269G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178269G>T , CM000673.2:g.89178269G>T	GRCh38
NC_000011.9:g.88911437G>T , CM000673.1:g.88911437G>T	GRCh37
NC_000011.8:g.88551085G>T	NCBI36
NG_008748.1:g.5398G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.316G>T MANE Select	ENSP00000263321.4:p.Gly106Cys
ENST00000263321.5:c.316G>T	ENSP00000263321.4:p.Gly106Cys
ENST00000526139.1:n.377G>T
NM_000372.4:c.316G>T	NP_000363.1:p.Gly106Cys
XM_011542970.1:c.316G>T	XP_011541272.1:p.Gly106Cys
XM_011542970.2:c.316G>T	XP_011541272.1:p.Gly106Cys
XR_001748321.1:n.2718-64736C>A
XR_001748322.1:n.2733-64736C>A
NM_000372.5:c.316G>T MANE Select	NP_000363.1:p.Gly106Cys