Canonical Allele Identifier: CA942404116
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1949710188
gnomAD v3: 11-113903461-CCTCT-C
gnomAD v4: 11-113903461-CCTCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903462_113903465del , CM000673.2:g.113903462_113903465del GRCh38
NC_000011.9:g.113774184_113774187del , CM000673.1:g.113774184_113774187del GRCh37
NC_000011.8:g.113279394_113279397del NCBI36
NG_011483.1:g.3596_3599del

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4379_12+4382del XP_011541366.1:n.12+4379_12+4382del
XM_024448767.1:c.-243+4379_-243+4382del XP_024304535.1:n.-243+4379_-243+4382del
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