Canonical Allele Identifier: CA2001397818

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932107_113932108delinsAC , CM000673.2:g.113932107_113932108delinsAC	GRCh38
NC_000011.9:g.113802829_113802830delinsAC , CM000673.1:g.113802829_113802830delinsAC	GRCh37
NC_000011.8:g.113308039_113308040delinsAC	NCBI36
NG_011483.1:g.32241_32242delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.369-182_369-181delinsAC MANE Select	ENSP00000260191.2:n.369-182_369-181delinsAC
ENST00000260191.7:c.369-182_369-181delinsAC	ENSP00000260191.2:n.369-182_369-181delinsAC
ENST00000260191.6:c.369-182_369-181delinsAC	ENSP00000260191.2:n.369-182_369-181delinsAC
ENST00000537778.5:c.336-182_336-181delinsAC	ENSP00000443118.1:n.336-182_336-181delinsAC
ENST00000543092.1:c.155-182_155-181delinsAC
NM_006028.4:c.369-182_369-181delinsAC	NP_006019.1:n.369-182_369-181delinsAC
XM_011543063.1:c.336-182_336-181delinsAC	XP_011541365.1:n.336-182_336-181delinsAC
XM_011543064.1:c.168-182_168-181delinsAC	XP_011541366.1:n.168-182_168-181delinsAC
XM_011543065.1:c.162-182_162-181delinsAC	XP_011541367.1:n.162-182_162-181delinsAC
XM_011543066.1:c.336-182_336-181delinsAC	XP_011541368.1:n.336-182_336-181delinsAC
NM_001363563.1:c.336-182_336-181delinsAC	NP_001350492.1:n.336-182_336-181delinsAC
XM_017018552.2:c.162-182_162-181delinsAC	XP_016874041.1:n.162-182_162-181delinsAC
XM_024448767.1:c.75-182_75-181delinsAC	XP_024304535.1:n.75-182_75-181delinsAC
XR_001748034.2:n.620-182_620-181delinsAC
NM_001363563.2:c.336-182_336-181delinsAC	NP_001350492.1:n.336-182_336-181delinsAC
NM_006028.5:c.369-182_369-181delinsAC MANE Select	NP_006019.1:n.369-182_369-181delinsAC