Canonical Allele Identifier: CA1948012671
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172196C= , CM000673.2:g.2172196C= GRCh38
NC_000011.9:g.2193426C= , CM000673.1:g.2193426C= GRCh37
NC_000011.8:g.2150002C= NCBI36
NG_008128.1:g.4610G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-410G= XP_011518637.1:n.-410G=