Canonical Allele Identifier: CA934420975
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1191522583
gnomAD v3: 11-2171883-C-A
gnomAD v4: 11-2171883-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171883C>A , CM000673.2:g.2171883C>A GRCh38
NC_000011.9:g.2193113C>A , CM000673.1:g.2193113C>A GRCh37
NC_000011.8:g.2149689C>A NCBI36
NG_008128.1:g.4923G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-97G>T XP_011518637.1:n.-97G>T
XM_011520335.2:c.-97G>T XP_011518637.1:n.-97G>T