Canonical Allele Identifier: CA2616054429

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932282-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932282C>A , CM000673.2:g.113932282C>A	GRCh38
NC_000011.9:g.113803004C>A , CM000673.1:g.113803004C>A	GRCh37
NC_000011.8:g.113308214C>A	NCBI36
NG_011483.1:g.32416C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.369-7C>A MANE Select	ENSP00000260191.2:n.369-7C>A
ENST00000260191.7:c.369-7C>A	ENSP00000260191.2:n.369-7C>A
ENST00000260191.6:c.369-7C>A	ENSP00000260191.2:n.369-7C>A
ENST00000537778.5:c.336-7C>A	ENSP00000443118.1:n.336-7C>A
ENST00000543092.1:c.155-7C>A
NM_006028.4:c.369-7C>A	NP_006019.1:n.369-7C>A
XM_011543063.1:c.336-7C>A	XP_011541365.1:n.336-7C>A
XM_011543064.1:c.168-7C>A	XP_011541366.1:n.168-7C>A
XM_011543065.1:c.162-7C>A	XP_011541367.1:n.162-7C>A
XM_011543066.1:c.336-7C>A	XP_011541368.1:n.336-7C>A
NM_001363563.1:c.336-7C>A	NP_001350492.1:n.336-7C>A
XM_017018552.2:c.162-7C>A	XP_016874041.1:n.162-7C>A
XM_024448767.1:c.75-7C>A	XP_024304535.1:n.75-7C>A
XR_001748034.2:n.620-7C>A
NM_001363563.2:c.336-7C>A	NP_001350492.1:n.336-7C>A
NM_006028.5:c.369-7C>A MANE Select	NP_006019.1:n.369-7C>A