Canonical Allele Identifier: CA382669134

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803137T>G (hg19) ; chr11:g.113932415T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932415T>G , CM000673.2:g.113932415T>G	GRCh38
NC_000011.9:g.113803137T>G , CM000673.1:g.113803137T>G	GRCh37
NC_000011.8:g.113308347T>G	NCBI36
NG_011483.1:g.32549T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.495T>G MANE Select	ENSP00000260191.2:p.Asp165Glu
ENST00000260191.7:c.495T>G	ENSP00000260191.2:p.Asp165Glu
ENST00000260191.6:c.495T>G	ENSP00000260191.2:p.Asp165Glu
ENST00000537778.5:c.462T>G	ENSP00000443118.1:p.Asp154Glu
ENST00000543092.1:c.281T>G
NM_006028.4:c.495T>G	NP_006019.1:p.Asp165Glu
XM_011543063.1:c.462T>G	XP_011541365.1:p.Asp154Glu
XM_011543064.1:c.294T>G	XP_011541366.1:p.Asp98Glu
XM_011543065.1:c.288T>G	XP_011541367.1:p.Asp96Glu
XM_011543066.1:c.462T>G	XP_011541368.1:p.Asp154Glu
NM_001363563.1:c.462T>G	NP_001350492.1:p.Asp154Glu
XM_017018552.2:c.288T>G	XP_016874041.1:p.Asp96Glu
XM_024448767.1:c.201T>G	XP_024304535.1:p.Asp67Glu
XR_001748034.2:n.746T>G
NM_001363563.2:c.462T>G	NP_001350492.1:p.Asp154Glu
NM_006028.5:c.495T>G MANE Select	NP_006019.1:p.Asp165Glu