Canonical Allele Identifier: CA228695605
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1040689912
gnomAD v3: 11-113903485-A-G
gnomAD v4: 11-113903485-A-G
MyVariant Identifiers: chr11:g.113774207A>G (hg19) chr11:g.113903485A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903485A>G , CM000673.2:g.113903485A>G GRCh38
NC_000011.9:g.113774207A>G , CM000673.1:g.113774207A>G GRCh37
NC_000011.8:g.113279417A>G NCBI36
NG_011483.1:g.3619A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4402A>G XP_011541366.1:n.12+4402A>G
XM_024448767.1:c.-243+4402A>G XP_024304535.1:n.-243+4402A>G
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