Canonical Allele Identifier: CA1948012298
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171916T= , CM000673.2:g.2171916T= GRCh38
NC_000011.9:g.2193146T= , CM000673.1:g.2193146T= GRCh37
NC_000011.8:g.2149722T= NCBI36
NG_008128.1:g.4890A=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-130A= XP_011518637.1:n.-130A=
XM_011520335.2:c.-130A= XP_011518637.1:n.-130A=