Canonical Allele Identifier: CA2001382900

Gene: HTR3B

Linked Data

• dbSNP Id: rs1949776928

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910225G>A , CM000673.2:g.113910225G>A	GRCh38
NC_000011.9:g.113780947G>A , CM000673.1:g.113780947G>A	GRCh37
NC_000011.8:g.113286157G>A	NCBI36
NG_011483.1:g.10359G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+770G>A MANE Select	ENSP00000260191.2:n.213+770G>A
ENST00000260191.7:c.213+770G>A	ENSP00000260191.2:n.213+770G>A
ENST00000260191.6:c.213+770G>A	ENSP00000260191.2:n.213+770G>A
ENST00000537778.5:c.180+770G>A	ENSP00000443118.1:n.180+770G>A
NM_006028.4:c.213+770G>A	NP_006019.1:n.213+770G>A
XM_011543063.1:c.180+770G>A	XP_011541365.1:n.180+770G>A
XM_011543064.1:c.12+11142G>A	XP_011541366.1:n.12+11142G>A
XM_011543066.1:c.180+770G>A	XP_011541368.1:n.180+770G>A
NM_001363563.1:c.180+770G>A	NP_001350492.1:n.180+770G>A
XM_024448767.1:c.-82+770G>A	XP_024304535.1:n.-82+770G>A
XR_001748034.2:n.464+770G>A
NM_001363563.2:c.180+770G>A	NP_001350492.1:n.180+770G>A
NM_006028.5:c.213+770G>A MANE Select	NP_006019.1:n.213+770G>A