Canonical Allele Identifier: CA1948012197
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171836C= , CM000673.2:g.2171836C= GRCh38
NC_000011.9:g.2193066C= , CM000673.1:g.2193066C= GRCh37
NC_000011.8:g.2149642C= NCBI36
NG_008128.1:g.4970G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000352909.7:c.-50G= ENSP00000325951.3:n.-50G=
XM_011520335.1:c.-50G= XP_011518637.1:n.-50G=
XM_011520335.2:c.-50G= XP_011518637.1:n.-50G=