Canonical Allele Identifier: CA2574983884

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932535-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932539del , CM000673.2:g.113932539del	GRCh38
NC_000011.9:g.113803261del , CM000673.1:g.113803261del	GRCh37
NC_000011.8:g.113308471del	NCBI36
NG_011483.1:g.32673del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+81del MANE Select	ENSP00000260191.2:n.538+81del
ENST00000260191.7:c.538+81del	ENSP00000260191.2:n.538+81del
ENST00000260191.6:c.538+81del	ENSP00000260191.2:n.538+81del
ENST00000537778.5:c.505+81del	ENSP00000443118.1:n.505+81del
ENST00000543092.1:c.324+81del
NM_006028.4:c.538+81del	NP_006019.1:n.538+81del
XM_011543063.1:c.505+81del	XP_011541365.1:n.505+81del
XM_011543064.1:c.337+81del	XP_011541366.1:n.337+81del
XM_011543065.1:c.331+81del	XP_011541367.1:n.331+81del
XM_011543066.1:c.505+81del	XP_011541368.1:n.505+81del
NM_001363563.1:c.505+81del	NP_001350492.1:n.505+81del
XM_017018552.2:c.331+81del	XP_016874041.1:n.331+81del
XM_024448767.1:c.244+81del	XP_024304535.1:n.244+81del
XR_001748034.2:n.789+81del
NM_001363563.2:c.505+81del	NP_001350492.1:n.505+81del
NM_006028.5:c.538+81del MANE Select	NP_006019.1:n.538+81del