Canonical Allele Identifier: CA476831472

Gene: HTR3B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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