Canonical Allele Identifier: CA2611984616
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2171891-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171891C>A , CM000673.2:g.2171891C>A GRCh38
NC_000011.9:g.2193121C>A , CM000673.1:g.2193121C>A GRCh37
NC_000011.8:g.2149697C>A NCBI36
NG_008128.1:g.4915G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-105G>T XP_011518637.1:n.-105G>T
XM_011520335.2:c.-105G>T XP_011518637.1:n.-105G>T