Canonical Allele Identifier: CA1948012182
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171829C= , CM000673.2:g.2171829C= GRCh38
NC_000011.9:g.2193059C= , CM000673.1:g.2193059C= GRCh37
NC_000011.8:g.2149635C= NCBI36
NG_008128.1:g.4977G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000352909.7:c.-43G= ENSP00000325951.3:n.-43G=
XM_011520335.1:c.-43G= XP_011518637.1:n.-43G=
XM_011520335.2:c.-43G= XP_011518637.1:n.-43G=