Canonical Allele Identifier: CA6284068

Gene: HTR3B

Linked Data

• dbSNP Id: rs756623079
• ExAC: 11:113803175 A / G
• gnomAD v2: 11-113803175-A-G
• gnomAD v4: 11-113932453-A-G
• MyVariant Identifiers: chr11:g.113803175A>G (hg19) ; chr11:g.113932453A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932453A>G , CM000673.2:g.113932453A>G	GRCh38
NC_000011.9:g.113803175A>G , CM000673.1:g.113803175A>G	GRCh37
NC_000011.8:g.113308385A>G	NCBI36
NG_011483.1:g.32587A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.533A>G MANE Select	ENSP00000260191.2:p.His178Arg
ENST00000260191.7:c.533A>G	ENSP00000260191.2:p.His178Arg
ENST00000260191.6:c.533A>G	ENSP00000260191.2:p.His178Arg
ENST00000537778.5:c.500A>G	ENSP00000443118.1:p.His167Arg
ENST00000543092.1:c.319A>G
NM_006028.4:c.533A>G	NP_006019.1:p.His178Arg
XM_011543063.1:c.500A>G	XP_011541365.1:p.His167Arg
XM_011543064.1:c.332A>G	XP_011541366.1:p.His111Arg
XM_011543065.1:c.326A>G	XP_011541367.1:p.His109Arg
XM_011543066.1:c.500A>G	XP_011541368.1:p.His167Arg
NM_001363563.1:c.500A>G	NP_001350492.1:p.His167Arg
XM_017018552.2:c.326A>G	XP_016874041.1:p.His109Arg
XM_024448767.1:c.239A>G	XP_024304535.1:p.His80Arg
XR_001748034.2:n.784A>G
NM_001363563.2:c.500A>G	NP_001350492.1:p.His167Arg
NM_006028.5:c.533A>G MANE Select	NP_006019.1:p.His178Arg