Canonical Allele Identifier: CA476831467

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803131A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932409A>C , CM000673.2:g.113932409A>C	GRCh38
NC_000011.9:g.113803131A>C , CM000673.1:g.113803131A>C	GRCh37
NC_000011.8:g.113308341A>C	NCBI36
NG_011483.1:g.32543A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.489A>C MANE Select	ENSP00000260191.2:p.Pro163=
ENST00000260191.7:c.489A>C	ENSP00000260191.2:p.Pro163=
ENST00000260191.6:c.489A>C	ENSP00000260191.2:p.Pro163=
ENST00000537778.5:c.456A>C	ENSP00000443118.1:p.Pro152=
ENST00000543092.1:c.275A>C
NM_006028.4:c.489A>C	NP_006019.1:p.Pro163=
XM_011543063.1:c.456A>C	XP_011541365.1:p.Pro152=
XM_011543064.1:c.288A>C	XP_011541366.1:p.Pro96=
XM_011543065.1:c.282A>C	XP_011541367.1:p.Pro94=
XM_011543066.1:c.456A>C	XP_011541368.1:p.Pro152=
NM_001363563.1:c.456A>C	NP_001350492.1:p.Pro152=
XM_017018552.2:c.282A>C	XP_016874041.1:p.Pro94=
XM_024448767.1:c.195A>C	XP_024304535.1:p.Pro65=
XR_001748034.2:n.740A>C
NM_001363563.2:c.456A>C	NP_001350492.1:p.Pro152=
NM_006028.5:c.489A>C MANE Select	NP_006019.1:p.Pro163=