Canonical Allele Identifier: CA6284058

Gene: HTR3B

Linked Data

• ClinVar Variation Id: 2210166
• ClinVar RCV Id: RCV002641780
• dbSNP Id: rs753847170
• ExAC: 11:113803109 G / A
• gnomAD v2: 11-113803109-G-A
• gnomAD v3: 11-113932387-G-A
• gnomAD v4: 11-113932387-G-A
• MyVariant Identifiers: chr11:g.113803109G>A (hg19) ; chr11:g.113932387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932387G>A , CM000673.2:g.113932387G>A	GRCh38
NC_000011.9:g.113803109G>A , CM000673.1:g.113803109G>A	GRCh37
NC_000011.8:g.113308319G>A	NCBI36
NG_011483.1:g.32521G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.467G>A MANE Select	ENSP00000260191.2:p.Ser156Asn
ENST00000260191.7:c.467G>A	ENSP00000260191.2:p.Ser156Asn
ENST00000260191.6:c.467G>A	ENSP00000260191.2:p.Ser156Asn
ENST00000537778.5:c.434G>A	ENSP00000443118.1:p.Ser145Asn
ENST00000543092.1:c.253G>A
NM_006028.4:c.467G>A	NP_006019.1:p.Ser156Asn
XM_011543063.1:c.434G>A	XP_011541365.1:p.Ser145Asn
XM_011543064.1:c.266G>A	XP_011541366.1:p.Ser89Asn
XM_011543065.1:c.260G>A	XP_011541367.1:p.Ser87Asn
XM_011543066.1:c.434G>A	XP_011541368.1:p.Ser145Asn
NM_001363563.1:c.434G>A	NP_001350492.1:p.Ser145Asn
XM_017018552.2:c.260G>A	XP_016874041.1:p.Ser87Asn
XM_024448767.1:c.173G>A	XP_024304535.1:p.Ser58Asn
XR_001748034.2:n.718G>A
NM_001363563.2:c.434G>A	NP_001350492.1:p.Ser145Asn
NM_006028.5:c.467G>A MANE Select	NP_006019.1:p.Ser156Asn