Canonical Allele Identifier: CA2723225674
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs2133705264

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172162C>T , CM000673.2:g.2172162C>T GRCh38
NC_000011.9:g.2193392C>T , CM000673.1:g.2193392C>T GRCh37
NC_000011.8:g.2149968C>T NCBI36
NG_008128.1:g.4644G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-376G>A XP_011518637.1:n.-376G>A