Canonical Allele Identifier: CA216230538
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs987040314
MyVariant Identifiers: chr11:g.2193315T>G (hg19) chr11:g.2172085T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172085T>G , CM000673.2:g.2172085T>G GRCh38
NC_000011.9:g.2193315T>G , CM000673.1:g.2193315T>G GRCh37
NC_000011.8:g.2149891T>G NCBI36
NG_008128.1:g.4721A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-299A>C XP_011518637.1:n.-299A>C
XM_011520335.2:c.-299A>C XP_011518637.1:n.-299A>C
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