Canonical Allele Identifier: CA671967120
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1311651746
gnomAD v3: 11-113903432-T-TC
gnomAD v4: 11-113903432-T-TC
MyVariant Identifiers: chr11:g.113774154_113774155insC (hg19) chr11:g.113903432_113903433insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903432_113903433insC , CM000673.2:g.113903432_113903433insC GRCh38
NC_000011.9:g.113774154_113774155insC , CM000673.1:g.113774154_113774155insC GRCh37
NC_000011.8:g.113279364_113279365insC NCBI36
NG_011483.1:g.3566_3567insC

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4349_12+4350insC XP_011541366.1:n.12+4349_12+4350insC
XM_024448767.1:c.-243+4349_-243+4350insC XP_024304535.1:n.-243+4349_-243+4350insC
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