Canonical Allele Identifier: CA2001382953

Gene: HTR3B

Linked Data

• dbSNP Id: rs1949778445

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910354A>G , CM000673.2:g.113910354A>G	GRCh38
NC_000011.9:g.113781076A>G , CM000673.1:g.113781076A>G	GRCh37
NC_000011.8:g.113286286A>G	NCBI36
NG_011483.1:g.10488A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.213+899A>G MANE Select	ENSP00000260191.2:n.213+899A>G
ENST00000260191.7:c.213+899A>G	ENSP00000260191.2:n.213+899A>G
ENST00000260191.6:c.213+899A>G	ENSP00000260191.2:n.213+899A>G
ENST00000537778.5:c.180+899A>G	ENSP00000443118.1:n.180+899A>G
NM_006028.4:c.213+899A>G	NP_006019.1:n.213+899A>G
XM_011543063.1:c.180+899A>G	XP_011541365.1:n.180+899A>G
XM_011543064.1:c.12+11271A>G	XP_011541366.1:n.12+11271A>G
XM_011543066.1:c.180+899A>G	XP_011541368.1:n.180+899A>G
NM_001363563.1:c.180+899A>G	NP_001350492.1:n.180+899A>G
XM_024448767.1:c.-82+899A>G	XP_024304535.1:n.-82+899A>G
XR_001748034.2:n.464+899A>G
NM_001363563.2:c.180+899A>G	NP_001350492.1:n.180+899A>G
NM_006028.5:c.213+899A>G MANE Select	NP_006019.1:n.213+899A>G