Canonical Allele Identifier: CA228695470
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs45492591
gnomAD v3: 11-113903286-C-A
gnomAD v4: 11-113903286-C-A
MyVariant Identifiers: chr11:g.113774008C>A (hg19) chr11:g.113903286C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903286C>A , CM000673.2:g.113903286C>A GRCh38
NC_000011.9:g.113774008C>A , CM000673.1:g.113774008C>A GRCh37
NC_000011.8:g.113279218C>A NCBI36
NG_011483.1:g.3420C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4203C>A XP_011541366.1:n.12+4203C>A
XM_024448767.1:c.-243+4203C>A XP_024304535.1:n.-243+4203C>A
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