Canonical Allele Identifier: CA1948012619
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172145G= , CM000673.2:g.2172145G= GRCh38
NC_000011.9:g.2193375G= , CM000673.1:g.2193375G= GRCh37
NC_000011.8:g.2149951G= NCBI36
NG_008128.1:g.4661C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-359C= XP_011518637.1:n.-359C=