Canonical Allele Identifier: CA671967137
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1404556064
gnomAD v3: 11-113903449-A-C
gnomAD v4: 11-113903449-A-C
MyVariant Identifiers: chr11:g.113774171A>C (hg19) chr11:g.113903449A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903449A>C , CM000673.2:g.113903449A>C GRCh38
NC_000011.9:g.113774171A>C , CM000673.1:g.113774171A>C GRCh37
NC_000011.8:g.113279381A>C NCBI36
NG_011483.1:g.3583A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4366A>C XP_011541366.1:n.12+4366A>C
XM_024448767.1:c.-243+4366A>C XP_024304535.1:n.-243+4366A>C
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