Canonical Allele Identifier: CA1948012630
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172165C= , CM000673.2:g.2172165C= GRCh38
NC_000011.9:g.2193395C= , CM000673.1:g.2193395C= GRCh37
NC_000011.8:g.2149971C= NCBI36
NG_008128.1:g.4641G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-379G= XP_011518637.1:n.-379G=