Canonical Allele Identifier: CA216230628
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs149761341
MyVariant Identifiers: chr11:g.2172174G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172174G>C , CM000673.2:g.2172174G>C GRCh38
NC_000011.9:g.2193404G>C , CM000673.1:g.2193404G>C GRCh37
NC_000011.8:g.2149980G>C NCBI36
NG_008128.1:g.4632C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-388C>G XP_011518637.1:n.-388C>G
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