Canonical Allele Identifier: CA601788451

Gene: HTR3B

Linked Data

• dbSNP Id: rs1159477829
• gnomAD v2: 11-113803309-G-GT
• gnomAD v3: 11-113932587-G-GT
• gnomAD v4: 11-113932587-G-GT
• MyVariant Identifiers: chr11:g.113803309_113803310insT (hg19) ; chr11:g.113932587_113932588insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932593dup , CM000673.2:g.113932593dup	GRCh38
NC_000011.9:g.113803315dup , CM000673.1:g.113803315dup	GRCh37
NC_000011.8:g.113308525dup	NCBI36
NG_011483.1:g.32727dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+135dup MANE Select	ENSP00000260191.2:n.538+135dup
ENST00000260191.7:c.538+135dup	ENSP00000260191.2:n.538+135dup
ENST00000260191.6:c.538+135dup	ENSP00000260191.2:n.538+135dup
ENST00000537778.5:c.505+135dup	ENSP00000443118.1:n.505+135dup
ENST00000543092.1:c.324+135dup
NM_006028.4:c.538+135dup	NP_006019.1:n.538+135dup
XM_011543063.1:c.505+135dup	XP_011541365.1:n.505+135dup
XM_011543064.1:c.337+135dup	XP_011541366.1:n.337+135dup
XM_011543065.1:c.331+135dup	XP_011541367.1:n.331+135dup
XM_011543066.1:c.505+135dup	XP_011541368.1:n.505+135dup
NM_001363563.1:c.505+135dup	NP_001350492.1:n.505+135dup
XM_017018552.2:c.331+135dup	XP_016874041.1:n.331+135dup
XM_024448767.1:c.244+135dup	XP_024304535.1:n.244+135dup
XR_001748034.2:n.789+135dup
NM_001363563.2:c.505+135dup	NP_001350492.1:n.505+135dup
NM_006028.5:c.538+135dup MANE Select	NP_006019.1:n.538+135dup