Canonical Allele Identifier: CA942404036
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1949709938
gnomAD v3: 11-113903447-TGA-T
gnomAD v4: 11-113903447-TGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903449_113903450del , CM000673.2:g.113903449_113903450del GRCh38
NC_000011.9:g.113774171_113774172del , CM000673.1:g.113774171_113774172del GRCh37
NC_000011.8:g.113279381_113279382del NCBI36
NG_011483.1:g.3583_3584del

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4366_12+4367del XP_011541366.1:n.12+4366_12+4367del
XM_024448767.1:c.-243+4366_-243+4367del XP_024304535.1:n.-243+4366_-243+4367del
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