Canonical Allele Identifier: CA1948012382
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171976C= , CM000673.2:g.2171976C= GRCh38
NC_000011.9:g.2193206C= , CM000673.1:g.2193206C= GRCh37
NC_000011.8:g.2149782C= NCBI36
NG_008128.1:g.4830G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-190G= XP_011518637.1:n.-190G=
XM_011520335.2:c.-190G= XP_011518637.1:n.-190G=