Canonical Allele Identifier: CA382669025

Gene: HTR3B

Linked Data

• dbSNP Id: rs764976973
• gnomAD v2: 11-113803117-A-G
• MyVariant Identifiers: chr11:g.113803117A>G (hg19) ; chr11:g.113932395A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932395A>G , CM000673.2:g.113932395A>G	GRCh38
NC_000011.9:g.113803117A>G , CM000673.1:g.113803117A>G	GRCh37
NC_000011.8:g.113308327A>G	NCBI36
NG_011483.1:g.32529A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.475A>G MANE Select	ENSP00000260191.2:p.Thr159Ala
ENST00000260191.7:c.475A>G	ENSP00000260191.2:p.Thr159Ala
ENST00000260191.6:c.475A>G	ENSP00000260191.2:p.Thr159Ala
ENST00000537778.5:c.442A>G	ENSP00000443118.1:p.Thr148Ala
ENST00000543092.1:c.261A>G
NM_006028.4:c.475A>G	NP_006019.1:p.Thr159Ala
XM_011543063.1:c.442A>G	XP_011541365.1:p.Thr148Ala
XM_011543064.1:c.274A>G	XP_011541366.1:p.Thr92Ala
XM_011543065.1:c.268A>G	XP_011541367.1:p.Thr90Ala
XM_011543066.1:c.442A>G	XP_011541368.1:p.Thr148Ala
NM_001363563.1:c.442A>G	NP_001350492.1:p.Thr148Ala
XM_017018552.2:c.268A>G	XP_016874041.1:p.Thr90Ala
XM_024448767.1:c.181A>G	XP_024304535.1:p.Thr61Ala
XR_001748034.2:n.726A>G
NM_001363563.2:c.442A>G	NP_001350492.1:p.Thr148Ala
NM_006028.5:c.475A>G MANE Select	NP_006019.1:p.Thr159Ala