Canonical Allele Identifier: CA1948012439
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1212488716
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172030G>T , CM000673.2:g.2172030G>T GRCh38
NC_000011.9:g.2193260G>T , CM000673.1:g.2193260G>T GRCh37
NC_000011.8:g.2149836G>T NCBI36
NG_008128.1:g.4776C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-244C>A XP_011518637.1:n.-244C>A
XM_011520335.2:c.-244C>A XP_011518637.1:n.-244C>A
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