Canonical Allele Identifier: CA382668720

Gene: HTR3B

Linked Data

• dbSNP Id: rs1409527052
• gnomAD v2: 11-113803035-C-A
• gnomAD v4: 11-113932313-C-A
• MyVariant Identifiers: chr11:g.113803035C>A (hg19) ; chr11:g.113932313C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932313C>A , CM000673.2:g.113932313C>A	GRCh38
NC_000011.9:g.113803035C>A , CM000673.1:g.113803035C>A	GRCh37
NC_000011.8:g.113308245C>A	NCBI36
NG_011483.1:g.32447C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.393C>A MANE Select	ENSP00000260191.2:p.Asp131Glu
ENST00000260191.7:c.393C>A	ENSP00000260191.2:p.Asp131Glu
ENST00000260191.6:c.393C>A	ENSP00000260191.2:p.Asp131Glu
ENST00000537778.5:c.360C>A	ENSP00000443118.1:p.Asp120Glu
ENST00000543092.1:c.179C>A
NM_006028.4:c.393C>A	NP_006019.1:p.Asp131Glu
XM_011543063.1:c.360C>A	XP_011541365.1:p.Asp120Glu
XM_011543064.1:c.192C>A	XP_011541366.1:p.Asp64Glu
XM_011543065.1:c.186C>A	XP_011541367.1:p.Asp62Glu
XM_011543066.1:c.360C>A	XP_011541368.1:p.Asp120Glu
NM_001363563.1:c.360C>A	NP_001350492.1:p.Asp120Glu
XM_017018552.2:c.186C>A	XP_016874041.1:p.Asp62Glu
XM_024448767.1:c.99C>A	XP_024304535.1:p.Asp33Glu
XR_001748034.2:n.644C>A
NM_001363563.2:c.360C>A	NP_001350492.1:p.Asp120Glu
NM_006028.5:c.393C>A MANE Select	NP_006019.1:p.Asp131Glu