Canonical Allele Identifier: CA671975812

Gene: HTR3B

Linked Data

• dbSNP Id: rs1186329696
• MyVariant Identifiers: chr11:g.113803371_113803372insGA (hg19) ; chr11:g.113932649_113932650insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932650_113932651dup , CM000673.2:g.113932650_113932651dup	GRCh38
NC_000011.9:g.113803372_113803373dup , CM000673.1:g.113803372_113803373dup	GRCh37
NC_000011.8:g.113308582_113308583dup	NCBI36
NG_011483.1:g.32784_32785dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+192_538+193dup MANE Select	ENSP00000260191.2:n.538+192_538+193dup
ENST00000260191.7:c.538+192_538+193dup	ENSP00000260191.2:n.538+192_538+193dup
ENST00000260191.6:c.538+192_538+193dup	ENSP00000260191.2:n.538+192_538+193dup
ENST00000537778.5:c.505+192_505+193dup	ENSP00000443118.1:n.505+192_505+193dup
ENST00000543092.1:c.324+192_324+193dup
NM_006028.4:c.538+192_538+193dup	NP_006019.1:n.538+192_538+193dup
XM_011543063.1:c.505+192_505+193dup	XP_011541365.1:n.505+192_505+193dup
XM_011543064.1:c.337+192_337+193dup	XP_011541366.1:n.337+192_337+193dup
XM_011543065.1:c.331+192_331+193dup	XP_011541367.1:n.331+192_331+193dup
XM_011543066.1:c.505+192_505+193dup	XP_011541368.1:n.505+192_505+193dup
NM_001363563.1:c.505+192_505+193dup	NP_001350492.1:n.505+192_505+193dup
XM_017018552.2:c.331+192_331+193dup	XP_016874041.1:n.331+192_331+193dup
XM_024448767.1:c.244+192_244+193dup	XP_024304535.1:n.244+192_244+193dup
XR_001748034.2:n.789+192_789+193dup
NM_001363563.2:c.505+192_505+193dup	NP_001350492.1:n.505+192_505+193dup
NM_006028.5:c.538+192_538+193dup MANE Select	NP_006019.1:n.538+192_538+193dup