Canonical Allele Identifier: CA653928697
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172145G>C , CM000673.2:g.2172145G>C GRCh38
NC_000011.9:g.2193375G>C , CM000673.1:g.2193375G>C GRCh37
NC_000011.8:g.2149951G>C NCBI36
NG_008128.1:g.4661C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-359C>G XP_011518637.1:n.-359C>G