Canonical Allele Identifier: CA382668558

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932287-A-G
• MyVariant Identifiers: chr11:g.113803009A>G (hg19) ; chr11:g.113932287A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932287A>G , CM000673.2:g.113932287A>G	GRCh38
NC_000011.9:g.113803009A>G , CM000673.1:g.113803009A>G	GRCh37
NC_000011.8:g.113308219A>G	NCBI36
NG_011483.1:g.32421A>G

Transcript Alleles

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