Canonical Allele Identifier: CA382669151

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803141C>G (hg19) ; chr11:g.113932419C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932419C>G , CM000673.2:g.113932419C>G	GRCh38
NC_000011.9:g.113803141C>G , CM000673.1:g.113803141C>G	GRCh37
NC_000011.8:g.113308351C>G	NCBI36
NG_011483.1:g.32553C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.499C>G MANE Select	ENSP00000260191.2:p.Gln167Glu
ENST00000260191.7:c.499C>G	ENSP00000260191.2:p.Gln167Glu
ENST00000260191.6:c.499C>G	ENSP00000260191.2:p.Gln167Glu
ENST00000537778.5:c.466C>G	ENSP00000443118.1:p.Gln156Glu
ENST00000543092.1:c.285C>G
NM_006028.4:c.499C>G	NP_006019.1:p.Gln167Glu
XM_011543063.1:c.466C>G	XP_011541365.1:p.Gln156Glu
XM_011543064.1:c.298C>G	XP_011541366.1:p.Gln100Glu
XM_011543065.1:c.292C>G	XP_011541367.1:p.Gln98Glu
XM_011543066.1:c.466C>G	XP_011541368.1:p.Gln156Glu
NM_001363563.1:c.466C>G	NP_001350492.1:p.Gln156Glu
XM_017018552.2:c.292C>G	XP_016874041.1:p.Gln98Glu
XM_024448767.1:c.205C>G	XP_024304535.1:p.Gln69Glu
XR_001748034.2:n.750C>G
NM_001363563.2:c.466C>G	NP_001350492.1:p.Gln156Glu
NM_006028.5:c.499C>G MANE Select	NP_006019.1:p.Gln167Glu