Canonical Allele Identifier: CA1948012587
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172119A= , CM000673.2:g.2172119A= GRCh38
NC_000011.9:g.2193349A= , CM000673.1:g.2193349A= GRCh37
NC_000011.8:g.2149925A= NCBI36
NG_008128.1:g.4687T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-333T= XP_011518637.1:n.-333T=
XM_011520335.2:c.-333T= XP_011518637.1:n.-333T=