Canonical Allele Identifier: CA934420976

Gene: TH

Linked Data

• dbSNP Id: rs1846271308
• gnomAD v3: 11-2171885-TC-T
• gnomAD v4: 11-2171885-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171889del , CM000673.2:g.2171889del	GRCh38
NC_000011.9:g.2193119del , CM000673.1:g.2193119del	GRCh37
NC_000011.8:g.2149695del	NCBI36
NG_008128.1:g.4920del

Transcript Alleles

HGVS	Amino-acid Change
XM_011520335.1:c.-100del	XP_011518637.1:n.-100del
XM_011520335.2:c.-100del	XP_011518637.1:n.-100del