Canonical Allele Identifier: CA228696628
Gene: HTR3B HGNC NCBI
gnomAD v2:
11:113775551 GAGA / G
gnomAD v3:
11:113904829 GAGA / G
gnomAD v4:
chr11-113904829-GAGA-G
Joint Max Group AF 0.20856615 (MID)
Genomes Max Group AF 0.13794039 (EAS)
Exomes Max Group AF 0.21064453 (MID)
dbSNP:
45460698
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113904832_113904834del , CM000673.2:g.113904832_113904834del GRCh38
NC_000011.9:g.113775554_113775556del , CM000673.1:g.113775554_113775556del GRCh37
NC_000011.8:g.113280764_113280766del NCBI36
NG_011483.1:g.4966_4968del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260191.8:c.-102_-100del MANE Select ENSP00000260191.2:n.-102_-100del
ENST00000260191.7:c.-102_-100del ENSP00000260191.2:n.-102_-100del
ENST00000260191.6:c.-102_-100del ENSP00000260191.2:n.-102_-100del
NM_006028.4:c.-102_-100del NP_006019.1:n.-102_-100del
XM_011543064.1:c.12+5749_12+5751del XP_011541366.1:n.12+5749_12+5751del
XM_024448767.1:c.-242-4463_-242-4461del XP_024304535.1:n.-242-4463_-242-4461del
NM_006028.5:c.-102_-100del MANE Select NP_006019.1:n.-102_-100del
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