Canonical Allele Identifier: CA942404001
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs57289369
gnomAD v3: 11-113903428-C-CTT
gnomAD v4: 11-113903428-C-CTT
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903446_113903447dup , CM000673.2:g.113903446_113903447dup GRCh38
NC_000011.9:g.113774168_113774169dup , CM000673.1:g.113774168_113774169dup GRCh37
NC_000011.8:g.113279378_113279379dup NCBI36
NG_011483.1:g.3580_3581dup

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4363_12+4364dup XP_011541366.1:n.12+4363_12+4364dup
XM_024448767.1:c.-243+4363_-243+4364dup XP_024304535.1:n.-243+4363_-243+4364dup
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