Canonical Allele Identifier: CA382668718

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803034A>T (hg19) ; chr11:g.113932312A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932312A>T , CM000673.2:g.113932312A>T	GRCh38
NC_000011.9:g.113803034A>T , CM000673.1:g.113803034A>T	GRCh37
NC_000011.8:g.113308244A>T	NCBI36
NG_011483.1:g.32446A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.392A>T MANE Select	ENSP00000260191.2:p.Asp131Val
ENST00000260191.7:c.392A>T	ENSP00000260191.2:p.Asp131Val
ENST00000260191.6:c.392A>T	ENSP00000260191.2:p.Asp131Val
ENST00000537778.5:c.359A>T	ENSP00000443118.1:p.Asp120Val
ENST00000543092.1:c.178A>T
NM_006028.4:c.392A>T	NP_006019.1:p.Asp131Val
XM_011543063.1:c.359A>T	XP_011541365.1:p.Asp120Val
XM_011543064.1:c.191A>T	XP_011541366.1:p.Asp64Val
XM_011543065.1:c.185A>T	XP_011541367.1:p.Asp62Val
XM_011543066.1:c.359A>T	XP_011541368.1:p.Asp120Val
NM_001363563.1:c.359A>T	NP_001350492.1:p.Asp120Val
XM_017018552.2:c.185A>T	XP_016874041.1:p.Asp62Val
XM_024448767.1:c.98A>T	XP_024304535.1:p.Asp33Val
XR_001748034.2:n.643A>T
NM_001363563.2:c.359A>T	NP_001350492.1:p.Asp120Val
NM_006028.5:c.392A>T MANE Select	NP_006019.1:p.Asp131Val