Canonical Allele Identifier: CA2616054347

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932153-C-CATGGAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932157_113932163dup , CM000673.2:g.113932157_113932163dup	GRCh38
NC_000011.9:g.113802879_113802885dup , CM000673.1:g.113802879_113802885dup	GRCh37
NC_000011.8:g.113308089_113308095dup	NCBI36
NG_011483.1:g.32291_32297dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.369-132_369-126dup MANE Select	ENSP00000260191.2:n.369-132_369-126dup
ENST00000260191.7:c.369-132_369-126dup	ENSP00000260191.2:n.369-132_369-126dup
ENST00000260191.6:c.369-132_369-126dup	ENSP00000260191.2:n.369-132_369-126dup
ENST00000537778.5:c.336-132_336-126dup	ENSP00000443118.1:n.336-132_336-126dup
ENST00000543092.1:c.155-132_155-126dup
NM_006028.4:c.369-132_369-126dup	NP_006019.1:n.369-132_369-126dup
XM_011543063.1:c.336-132_336-126dup	XP_011541365.1:n.336-132_336-126dup
XM_011543064.1:c.168-132_168-126dup	XP_011541366.1:n.168-132_168-126dup
XM_011543065.1:c.162-132_162-126dup	XP_011541367.1:n.162-132_162-126dup
XM_011543066.1:c.336-132_336-126dup	XP_011541368.1:n.336-132_336-126dup
NM_001363563.1:c.336-132_336-126dup	NP_001350492.1:n.336-132_336-126dup
XM_017018552.2:c.162-132_162-126dup	XP_016874041.1:n.162-132_162-126dup
XM_024448767.1:c.75-132_75-126dup	XP_024304535.1:n.75-132_75-126dup
XR_001748034.2:n.620-132_620-126dup
NM_001363563.2:c.336-132_336-126dup	NP_001350492.1:n.336-132_336-126dup
NM_006028.5:c.369-132_369-126dup MANE Select	NP_006019.1:n.369-132_369-126dup