Canonical Allele Identifier: CA1948012322
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171935G= , CM000673.2:g.2171935G= GRCh38
NC_000011.9:g.2193165G= , CM000673.1:g.2193165G= GRCh37
NC_000011.8:g.2149741G= NCBI36
NG_008128.1:g.4871C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-149C= XP_011518637.1:n.-149C=
XM_011520335.2:c.-149C= XP_011518637.1:n.-149C=