Canonical Allele Identifier: CA476831334

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803095G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932373G>C , CM000673.2:g.113932373G>C	GRCh38
NC_000011.9:g.113803095G>C , CM000673.1:g.113803095G>C	GRCh37
NC_000011.8:g.113308305G>C	NCBI36
NG_011483.1:g.32507G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.453G>C MANE Select	ENSP00000260191.2:p.Val151=
ENST00000260191.7:c.453G>C	ENSP00000260191.2:p.Val151=
ENST00000260191.6:c.453G>C	ENSP00000260191.2:p.Val151=
ENST00000537778.5:c.420G>C	ENSP00000443118.1:p.Val140=
ENST00000543092.1:c.239G>C
NM_006028.4:c.453G>C	NP_006019.1:p.Val151=
XM_011543063.1:c.420G>C	XP_011541365.1:p.Val140=
XM_011543064.1:c.252G>C	XP_011541366.1:p.Val84=
XM_011543065.1:c.246G>C	XP_011541367.1:p.Val82=
XM_011543066.1:c.420G>C	XP_011541368.1:p.Val140=
NM_001363563.1:c.420G>C	NP_001350492.1:p.Val140=
XM_017018552.2:c.246G>C	XP_016874041.1:p.Val82=
XM_024448767.1:c.159G>C	XP_024304535.1:p.Val53=
XR_001748034.2:n.704G>C
NM_001363563.2:c.420G>C	NP_001350492.1:p.Val140=
NM_006028.5:c.453G>C MANE Select	NP_006019.1:p.Val151=