Canonical Allele Identifier: CA942420363

Gene: HTR3B

Linked Data

• dbSNP Id: rs1950048247
• gnomAD v3: 11-113932651-A-AG
• gnomAD v4: 11-113932651-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932651_113932652insG , CM000673.2:g.113932651_113932652insG	GRCh38
NC_000011.9:g.113803373_113803374insG , CM000673.1:g.113803373_113803374insG	GRCh37
NC_000011.8:g.113308583_113308584insG	NCBI36
NG_011483.1:g.32785_32786insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+193_538+194insG MANE Select	ENSP00000260191.2:n.538+193_538+194insG
ENST00000260191.7:c.538+193_538+194insG	ENSP00000260191.2:n.538+193_538+194insG
ENST00000260191.6:c.538+193_538+194insG	ENSP00000260191.2:n.538+193_538+194insG
ENST00000537778.5:c.505+193_505+194insG	ENSP00000443118.1:n.505+193_505+194insG
ENST00000543092.1:c.324+193_324+194insG
NM_006028.4:c.538+193_538+194insG	NP_006019.1:n.538+193_538+194insG
XM_011543063.1:c.505+193_505+194insG	XP_011541365.1:n.505+193_505+194insG
XM_011543064.1:c.337+193_337+194insG	XP_011541366.1:n.337+193_337+194insG
XM_011543065.1:c.331+193_331+194insG	XP_011541367.1:n.331+193_331+194insG
XM_011543066.1:c.505+193_505+194insG	XP_011541368.1:n.505+193_505+194insG
NM_001363563.1:c.505+193_505+194insG	NP_001350492.1:n.505+193_505+194insG
XM_017018552.2:c.331+193_331+194insG	XP_016874041.1:n.331+193_331+194insG
XM_024448767.1:c.244+193_244+194insG	XP_024304535.1:n.244+193_244+194insG
XR_001748034.2:n.789+193_789+194insG
NM_001363563.2:c.505+193_505+194insG	NP_001350492.1:n.505+193_505+194insG
NM_006028.5:c.538+193_538+194insG MANE Select	NP_006019.1:n.538+193_538+194insG