Canonical Allele Identifier: CA674605648
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172610A>C , CM000673.2:g.2172610A>C GRCh38
NC_000011.9:g.2193840A>C , CM000673.1:g.2193840A>C GRCh37
NC_000011.8:g.2150416A>C NCBI36
NG_008128.1:g.4196T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-824T>G XP_011518637.1:n.-824T>G