Canonical Allele Identifier: CA1948012351
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1846272837
gnomAD v4: 11-2171955-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171955G>A , CM000673.2:g.2171955G>A GRCh38
NC_000011.9:g.2193185G>A , CM000673.1:g.2193185G>A GRCh37
NC_000011.8:g.2149761G>A NCBI36
NG_008128.1:g.4851C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-169C>T XP_011518637.1:n.-169C>T
XM_011520335.2:c.-169C>T XP_011518637.1:n.-169C>T
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