Canonical Allele Identifier: CA476831240

Gene: HTR3B

Linked Data

• COSMIC: COSM3967325
• MyVariant Identifiers: chr11:g.113803068C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932346C>A , CM000673.2:g.113932346C>A	GRCh38
NC_000011.9:g.113803068C>A , CM000673.1:g.113803068C>A	GRCh37
NC_000011.8:g.113308278C>A	NCBI36
NG_011483.1:g.32480C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.426C>A MANE Select	ENSP00000260191.2:p.Thr142=
ENST00000260191.7:c.426C>A	ENSP00000260191.2:p.Thr142=
ENST00000260191.6:c.426C>A	ENSP00000260191.2:p.Thr142=
ENST00000537778.5:c.393C>A	ENSP00000443118.1:p.Thr131=
ENST00000543092.1:c.212C>A
NM_006028.4:c.426C>A	NP_006019.1:p.Thr142=
XM_011543063.1:c.393C>A	XP_011541365.1:p.Thr131=
XM_011543064.1:c.225C>A	XP_011541366.1:p.Thr75=
XM_011543065.1:c.219C>A	XP_011541367.1:p.Thr73=
XM_011543066.1:c.393C>A	XP_011541368.1:p.Thr131=
NM_001363563.1:c.393C>A	NP_001350492.1:p.Thr131=
XM_017018552.2:c.219C>A	XP_016874041.1:p.Thr73=
XM_024448767.1:c.132C>A	XP_024304535.1:p.Thr44=
XR_001748034.2:n.677C>A
NM_001363563.2:c.393C>A	NP_001350492.1:p.Thr131=
NM_006028.5:c.426C>A MANE Select	NP_006019.1:p.Thr142=