Canonical Allele Identifier: CA2001382897

Gene: HTR3B

Linked Data

• dbSNP Id: rs1949776853

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910221G>T , CM000673.2:g.113910221G>T	GRCh38
NC_000011.9:g.113780943G>T , CM000673.1:g.113780943G>T	GRCh37
NC_000011.8:g.113286153G>T	NCBI36
NG_011483.1:g.10355G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+766G>T MANE Select	ENSP00000260191.2:n.213+766G>T
ENST00000260191.7:c.213+766G>T	ENSP00000260191.2:n.213+766G>T
ENST00000260191.6:c.213+766G>T	ENSP00000260191.2:n.213+766G>T
ENST00000537778.5:c.180+766G>T	ENSP00000443118.1:n.180+766G>T
NM_006028.4:c.213+766G>T	NP_006019.1:n.213+766G>T
XM_011543063.1:c.180+766G>T	XP_011541365.1:n.180+766G>T
XM_011543064.1:c.12+11138G>T	XP_011541366.1:n.12+11138G>T
XM_011543066.1:c.180+766G>T	XP_011541368.1:n.180+766G>T
NM_001363563.1:c.180+766G>T	NP_001350492.1:n.180+766G>T
XM_024448767.1:c.-82+766G>T	XP_024304535.1:n.-82+766G>T
XR_001748034.2:n.464+766G>T
NM_001363563.2:c.180+766G>T	NP_001350492.1:n.180+766G>T
NM_006028.5:c.213+766G>T MANE Select	NP_006019.1:n.213+766G>T