Canonical Allele Identifier: CA1948012310

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171931_2171932delinsCG , CM000673.2:g.2171931_2171932delinsCG	GRCh38
NC_000011.9:g.2193161_2193162delinsCG , CM000673.1:g.2193161_2193162delinsCG	GRCh37
NC_000011.8:g.2149737_2149738delinsCG	NCBI36
NG_008128.1:g.4874_4875delinsCG

Transcript Alleles

HGVS	Amino-acid Change
XM_011520335.1:c.-146_-145delinsCG	XP_011518637.1:n.-146_-145delinsCG
XM_011520335.2:c.-146_-145delinsCG	XP_011518637.1:n.-146_-145delinsCG