Canonical Allele Identifier: CA942406459

Gene: HTR3B

Linked Data

• dbSNP Id: rs1035071732
• gnomAD v3: 11-113910202-T-C
• gnomAD v4: 11-113910202-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910202T>C , CM000673.2:g.113910202T>C	GRCh38
NC_000011.9:g.113780924T>C , CM000673.1:g.113780924T>C	GRCh37
NC_000011.8:g.113286134T>C	NCBI36
NG_011483.1:g.10336T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+747T>C MANE Select	ENSP00000260191.2:n.213+747T>C
ENST00000260191.7:c.213+747T>C	ENSP00000260191.2:n.213+747T>C
ENST00000260191.6:c.213+747T>C	ENSP00000260191.2:n.213+747T>C
ENST00000537778.5:c.180+747T>C	ENSP00000443118.1:n.180+747T>C
NM_006028.4:c.213+747T>C	NP_006019.1:n.213+747T>C
XM_011543063.1:c.180+747T>C	XP_011541365.1:n.180+747T>C
XM_011543064.1:c.12+11119T>C	XP_011541366.1:n.12+11119T>C
XM_011543066.1:c.180+747T>C	XP_011541368.1:n.180+747T>C
NM_001363563.1:c.180+747T>C	NP_001350492.1:n.180+747T>C
XM_024448767.1:c.-82+747T>C	XP_024304535.1:n.-82+747T>C
XR_001748034.2:n.464+747T>C
NM_001363563.2:c.180+747T>C	NP_001350492.1:n.180+747T>C
NM_006028.5:c.213+747T>C MANE Select	NP_006019.1:n.213+747T>C