Canonical Allele Identifier: CA942403794
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1949708433
gnomAD v3: 11-113903316-T-A
gnomAD v4: 11-113903316-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903316T>A , CM000673.2:g.113903316T>A GRCh38
NC_000011.9:g.113774038T>A , CM000673.1:g.113774038T>A GRCh37
NC_000011.8:g.113279248T>A NCBI36
NG_011483.1:g.3450T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4233T>A XP_011541366.1:n.12+4233T>A
XM_024448767.1:c.-243+4233T>A XP_024304535.1:n.-243+4233T>A
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