Canonical Allele Identifier: CA942420370

Gene: HTR3B

Linked Data

• dbSNP Id: rs1950048321
• gnomAD v3: 11-113932652-A-AC
• gnomAD v4: 11-113932652-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932652_113932653insC , CM000673.2:g.113932652_113932653insC	GRCh38
NC_000011.9:g.113803374_113803375insC , CM000673.1:g.113803374_113803375insC	GRCh37
NC_000011.8:g.113308584_113308585insC	NCBI36
NG_011483.1:g.32786_32787insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+194_538+195insC MANE Select	ENSP00000260191.2:n.538+194_538+195insC
ENST00000260191.7:c.538+194_538+195insC	ENSP00000260191.2:n.538+194_538+195insC
ENST00000260191.6:c.538+194_538+195insC	ENSP00000260191.2:n.538+194_538+195insC
ENST00000537778.5:c.505+194_505+195insC	ENSP00000443118.1:n.505+194_505+195insC
ENST00000543092.1:c.324+194_324+195insC
NM_006028.4:c.538+194_538+195insC	NP_006019.1:n.538+194_538+195insC
XM_011543063.1:c.505+194_505+195insC	XP_011541365.1:n.505+194_505+195insC
XM_011543064.1:c.337+194_337+195insC	XP_011541366.1:n.337+194_337+195insC
XM_011543065.1:c.331+194_331+195insC	XP_011541367.1:n.331+194_331+195insC
XM_011543066.1:c.505+194_505+195insC	XP_011541368.1:n.505+194_505+195insC
NM_001363563.1:c.505+194_505+195insC	NP_001350492.1:n.505+194_505+195insC
XM_017018552.2:c.331+194_331+195insC	XP_016874041.1:n.331+194_331+195insC
XM_024448767.1:c.244+194_244+195insC	XP_024304535.1:n.244+194_244+195insC
XR_001748034.2:n.789+194_789+195insC
NM_001363563.2:c.505+194_505+195insC	NP_001350492.1:n.505+194_505+195insC
NM_006028.5:c.538+194_538+195insC MANE Select	NP_006019.1:n.538+194_538+195insC