Canonical Allele Identifier: CA1948012635
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1846278085

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172167G>A , CM000673.2:g.2172167G>A GRCh38
NC_000011.9:g.2193397G>A , CM000673.1:g.2193397G>A GRCh37
NC_000011.8:g.2149973G>A NCBI36
NG_008128.1:g.4639C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-381C>T XP_011518637.1:n.-381C>T