Canonical Allele Identifier: CA1948012874
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172367C>A , CM000673.2:g.2172367C>A GRCh38
NC_000011.9:g.2193597C>A , CM000673.1:g.2193597C>A GRCh37
NC_000011.8:g.2150173C>A NCBI36
NG_008128.1:g.4439G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-581G>T XP_011518637.1:n.-581G>T