Canonical Allele Identifier: CA2616054359

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932167-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932169_113932170del , CM000673.2:g.113932169_113932170del	GRCh38
NC_000011.9:g.113802891_113802892del , CM000673.1:g.113802891_113802892del	GRCh37
NC_000011.8:g.113308101_113308102del	NCBI36
NG_011483.1:g.32303_32304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.369-120_369-119del MANE Select	ENSP00000260191.2:n.369-120_369-119del
ENST00000260191.7:c.369-120_369-119del	ENSP00000260191.2:n.369-120_369-119del
ENST00000260191.6:c.369-120_369-119del	ENSP00000260191.2:n.369-120_369-119del
ENST00000537778.5:c.336-120_336-119del	ENSP00000443118.1:n.336-120_336-119del
ENST00000543092.1:c.155-120_155-119del
NM_006028.4:c.369-120_369-119del	NP_006019.1:n.369-120_369-119del
XM_011543063.1:c.336-120_336-119del	XP_011541365.1:n.336-120_336-119del
XM_011543064.1:c.168-120_168-119del	XP_011541366.1:n.168-120_168-119del
XM_011543065.1:c.162-120_162-119del	XP_011541367.1:n.162-120_162-119del
XM_011543066.1:c.336-120_336-119del	XP_011541368.1:n.336-120_336-119del
NM_001363563.1:c.336-120_336-119del	NP_001350492.1:n.336-120_336-119del
XM_017018552.2:c.162-120_162-119del	XP_016874041.1:n.162-120_162-119del
XM_024448767.1:c.75-120_75-119del	XP_024304535.1:n.75-120_75-119del
XR_001748034.2:n.620-120_620-119del
NM_001363563.2:c.336-120_336-119del	NP_001350492.1:n.336-120_336-119del
NM_006028.5:c.369-120_369-119del MANE Select	NP_006019.1:n.369-120_369-119del