Canonical Allele Identifier: CA228668336

Gene: HTR3B

Linked Data

• dbSNP Id: rs2307599
• gnomAD v2: 11-113803374-A-AAC
• gnomAD v3: 11-113932652-A-AAC
• gnomAD v4: 11-113932652-A-AAC
• MyVariant Identifiers: chr11:g.113803375_113803376insCA (hg19) ; chr11:g.113803374_113803375insAC (hg19) ; chr11:g.113932653_113932654insCA (hg38) ; chr11:g.113932652_113932653insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932654_113932655dup , CM000673.2:g.113932654_113932655dup	GRCh38
NC_000011.9:g.113803376_113803377dup , CM000673.1:g.113803376_113803377dup	GRCh37
NC_000011.8:g.113308586_113308587dup	NCBI36
NG_011483.1:g.32788_32789dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+196_538+197dup MANE Select	ENSP00000260191.2:n.538+196_538+197dup
ENST00000260191.7:c.538+196_538+197dup	ENSP00000260191.2:n.538+196_538+197dup
ENST00000260191.6:c.538+196_538+197dup	ENSP00000260191.2:n.538+196_538+197dup
ENST00000537778.5:c.505+196_505+197dup	ENSP00000443118.1:n.505+196_505+197dup
ENST00000543092.1:c.324+196_324+197dup
NM_006028.4:c.538+196_538+197dup	NP_006019.1:n.538+196_538+197dup
XM_011543063.1:c.505+196_505+197dup	XP_011541365.1:n.505+196_505+197dup
XM_011543064.1:c.337+196_337+197dup	XP_011541366.1:n.337+196_337+197dup
XM_011543065.1:c.331+196_331+197dup	XP_011541367.1:n.331+196_331+197dup
XM_011543066.1:c.505+196_505+197dup	XP_011541368.1:n.505+196_505+197dup
NM_001363563.1:c.505+196_505+197dup	NP_001350492.1:n.505+196_505+197dup
XM_017018552.2:c.331+196_331+197dup	XP_016874041.1:n.331+196_331+197dup
XM_024448767.1:c.244+196_244+197dup	XP_024304535.1:n.244+196_244+197dup
XR_001748034.2:n.789+196_789+197dup
NM_001363563.2:c.505+196_505+197dup	NP_001350492.1:n.505+196_505+197dup
NM_006028.5:c.538+196_538+197dup MANE Select	NP_006019.1:n.538+196_538+197dup