Canonical Allele Identifier: CA1948012345
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171950A= , CM000673.2:g.2171950A= GRCh38
NC_000011.9:g.2193180A= , CM000673.1:g.2193180A= GRCh37
NC_000011.8:g.2149756A= NCBI36
NG_008128.1:g.4856T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-164T= XP_011518637.1:n.-164T=
XM_011520335.2:c.-164T= XP_011518637.1:n.-164T=