Canonical Allele Identifier: CA1948012651
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1846278293
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172179A>G , CM000673.2:g.2172179A>G GRCh38
NC_000011.9:g.2193409A>G , CM000673.1:g.2193409A>G GRCh37
NC_000011.8:g.2149985A>G NCBI36
NG_008128.1:g.4627T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-393T>C XP_011518637.1:n.-393T>C
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