Canonical Allele Identifier: CA1948012649
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172179A= , CM000673.2:g.2172179A= GRCh38
NC_000011.9:g.2193409A= , CM000673.1:g.2193409A= GRCh37
NC_000011.8:g.2149985A= NCBI36
NG_008128.1:g.4627T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-393T= XP_011518637.1:n.-393T=