Canonical Allele Identifier: CA228695608
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs915295983
gnomAD v3: 11-113903491-G-A
gnomAD v4: 11-113903491-G-A
MyVariant Identifiers: chr11:g.113774213G>A (hg19) chr11:g.113903491G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903491G>A , CM000673.2:g.113903491G>A GRCh38
NC_000011.9:g.113774213G>A , CM000673.1:g.113774213G>A GRCh37
NC_000011.8:g.113279423G>A NCBI36
NG_011483.1:g.3625G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4408G>A XP_011541366.1:n.12+4408G>A
XM_024448767.1:c.-243+4408G>A XP_024304535.1:n.-243+4408G>A
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