Canonical Allele Identifier: CA6284047

Gene: HTR3B

Linked Data

• ClinVar Variation Id: 2401467
• ClinVar RCV Id: RCV004234319
• dbSNP Id: rs150009887
• ExAC: 11:113803087 A / G
• gnomAD v2: 11-113803087-A-G
• gnomAD v3: 11-113932365-A-G
• gnomAD v4: 11-113932365-A-G
• MyVariant Identifiers: chr11:g.113803087A>G (hg19) ; chr11:g.113932365A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932365A>G , CM000673.2:g.113932365A>G	GRCh38
NC_000011.9:g.113803087A>G , CM000673.1:g.113803087A>G	GRCh37
NC_000011.8:g.113308297A>G	NCBI36
NG_011483.1:g.32499A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.445A>G MANE Select	ENSP00000260191.2:p.Ile149Val
ENST00000260191.7:c.445A>G	ENSP00000260191.2:p.Ile149Val
ENST00000260191.6:c.445A>G	ENSP00000260191.2:p.Ile149Val
ENST00000537778.5:c.412A>G	ENSP00000443118.1:p.Ile138Val
ENST00000543092.1:c.231A>G
NM_006028.4:c.445A>G	NP_006019.1:p.Ile149Val
XM_011543063.1:c.412A>G	XP_011541365.1:p.Ile138Val
XM_011543064.1:c.244A>G	XP_011541366.1:p.Ile82Val
XM_011543065.1:c.238A>G	XP_011541367.1:p.Ile80Val
XM_011543066.1:c.412A>G	XP_011541368.1:p.Ile138Val
NM_001363563.1:c.412A>G	NP_001350492.1:p.Ile138Val
XM_017018552.2:c.238A>G	XP_016874041.1:p.Ile80Val
XM_024448767.1:c.151A>G	XP_024304535.1:p.Ile51Val
XR_001748034.2:n.696A>G
NM_001363563.2:c.412A>G	NP_001350492.1:p.Ile138Val
NM_006028.5:c.445A>G MANE Select	NP_006019.1:p.Ile149Val