Canonical Allele Identifier: CA2611984622

Gene: TH

Linked Data

• gnomAD v4: 11-2171892-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171894del , CM000673.2:g.2171894del	GRCh38
NC_000011.9:g.2193124del , CM000673.1:g.2193124del	GRCh37
NC_000011.8:g.2149700del	NCBI36
NG_008128.1:g.4913del

Transcript Alleles

HGVS	Amino-acid Change
XM_011520335.1:c.-107del	XP_011518637.1:n.-107del
XM_011520335.2:c.-107del	XP_011518637.1:n.-107del