Canonical Allele Identifier: CA1948012466
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172039C= , CM000673.2:g.2172039C= GRCh38
NC_000011.9:g.2193269C= , CM000673.1:g.2193269C= GRCh37
NC_000011.8:g.2149845C= NCBI36
NG_008128.1:g.4767G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-253G= XP_011518637.1:n.-253G=
XM_011520335.2:c.-253G= XP_011518637.1:n.-253G=