Canonical Allele Identifier: CA1948012392
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171980G= , CM000673.2:g.2171980G= GRCh38
NC_000011.9:g.2193210G= , CM000673.1:g.2193210G= GRCh37
NC_000011.8:g.2149786G= NCBI36
NG_008128.1:g.4826C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-194C= XP_011518637.1:n.-194C=
XM_011520335.2:c.-194C= XP_011518637.1:n.-194C=