Canonical Allele Identifier: CA2611984920
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2171977-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171977C>A , CM000673.2:g.2171977C>A GRCh38
NC_000011.9:g.2193207C>A , CM000673.1:g.2193207C>A GRCh37
NC_000011.8:g.2149783C>A NCBI36
NG_008128.1:g.4829G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-191G>T XP_011518637.1:n.-191G>T
XM_011520335.2:c.-191G>T XP_011518637.1:n.-191G>T