Canonical Allele Identifier: CA674605244

Gene: TH

Linked Data

• dbSNP Id: rs1375095062
• MyVariant Identifiers: chr11:g.2193275C>T (hg19) ; chr11:g.2172045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2172045C>T , CM000673.2:g.2172045C>T	GRCh38
NC_000011.9:g.2193275C>T , CM000673.1:g.2193275C>T	GRCh37
NC_000011.8:g.2149851C>T	NCBI36
NG_008128.1:g.4761G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011520335.1:c.-259G>A	XP_011518637.1:n.-259G>A
XM_011520335.2:c.-259G>A	XP_011518637.1:n.-259G>A