Canonical Allele Identifier: CA1948012642
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172174G= , CM000673.2:g.2172174G= GRCh38
NC_000011.9:g.2193404G= , CM000673.1:g.2193404G= GRCh37
NC_000011.8:g.2149980G= NCBI36
NG_008128.1:g.4632C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-388C= XP_011518637.1:n.-388C=