Canonical Allele Identifier: CA1948012304
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171919G= , CM000673.2:g.2171919G= GRCh38
NC_000011.9:g.2193149G= , CM000673.1:g.2193149G= GRCh37
NC_000011.8:g.2149725G= NCBI36
NG_008128.1:g.4887C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-133C= XP_011518637.1:n.-133C=
XM_011520335.2:c.-133C= XP_011518637.1:n.-133C=