Canonical Allele Identifier: CA2001398089

Gene: HTR3B

Linked Data

• dbSNP Id: rs1950047784

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932633_113932637dup , CM000673.2:g.113932633_113932637dup	GRCh38
NC_000011.9:g.113803355_113803359dup , CM000673.1:g.113803355_113803359dup	GRCh37
NC_000011.8:g.113308565_113308569dup	NCBI36
NG_011483.1:g.32767_32771dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+175_538+179dup MANE Select	ENSP00000260191.2:n.538+175_538+179dup
ENST00000260191.7:c.538+175_538+179dup	ENSP00000260191.2:n.538+175_538+179dup
ENST00000260191.6:c.538+175_538+179dup	ENSP00000260191.2:n.538+175_538+179dup
ENST00000537778.5:c.505+175_505+179dup	ENSP00000443118.1:n.505+175_505+179dup
ENST00000543092.1:c.324+175_324+179dup
NM_006028.4:c.538+175_538+179dup	NP_006019.1:n.538+175_538+179dup
XM_011543063.1:c.505+175_505+179dup	XP_011541365.1:n.505+175_505+179dup
XM_011543064.1:c.337+175_337+179dup	XP_011541366.1:n.337+175_337+179dup
XM_011543065.1:c.331+175_331+179dup	XP_011541367.1:n.331+175_331+179dup
XM_011543066.1:c.505+175_505+179dup	XP_011541368.1:n.505+175_505+179dup
NM_001363563.1:c.505+175_505+179dup	NP_001350492.1:n.505+175_505+179dup
XM_017018552.2:c.331+175_331+179dup	XP_016874041.1:n.331+175_331+179dup
XM_024448767.1:c.244+175_244+179dup	XP_024304535.1:n.244+175_244+179dup
XR_001748034.2:n.789+175_789+179dup
NM_001363563.2:c.505+175_505+179dup	NP_001350492.1:n.505+175_505+179dup
NM_006028.5:c.538+175_538+179dup MANE Select	NP_006019.1:n.538+175_538+179dup