Canonical Allele Identifier: CA382668675

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932306A>G , CM000673.2:g.113932306A>G	GRCh38
NC_000011.9:g.113803028A>G , CM000673.1:g.113803028A>G	GRCh37
NC_000011.8:g.113308238A>G	NCBI36
NG_011483.1:g.32440A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006028.5:c.386A>G MANE Select	NP_006019.1:p.Tyr129Cys
ENST00000260191.8:c.386A>G MANE Select	ENSP00000260191.2:p.Tyr129Cys
NM_001363563.1:c.353A>G	NP_001350492.1:p.Tyr118Cys
NM_001363563.2:c.353A>G	NP_001350492.1:p.Tyr118Cys
NM_006028.4:c.386A>G	NP_006019.1:p.Tyr129Cys
ENST00000260191.6:c.386A>G	ENSP00000260191.2:p.Tyr129Cys
ENST00000260191.7:c.386A>G	ENSP00000260191.2:p.Tyr129Cys
ENST00000537778.5:c.353A>G	ENSP00000443118.1:p.Tyr118Cys
ENST00000543092.1:c.172A>G
XM_011543063.1:c.353A>G	XP_011541365.1:p.Tyr118Cys
XM_011543064.1:c.185A>G	XP_011541366.1:p.Tyr62Cys
XM_011543065.1:c.179A>G	XP_011541367.1:p.Tyr60Cys
XM_011543066.1:c.353A>G	XP_011541368.1:p.Tyr118Cys
XM_017018552.2:c.179A>G	XP_016874041.1:p.Tyr60Cys
XM_024448767.1:c.92A>G	XP_024304535.1:p.Tyr31Cys
XR_001748034.2:n.637A>G