Canonical Allele Identifier: CA228668356

Gene: HTR3B

Linked Data

• dbSNP Id: rs1555110014
• MyVariant Identifiers: chr11:g.113803375_113803376insAC (hg19) ; chr11:g.113932653_113932654insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932653_113932654insAC , CM000673.2:g.113932653_113932654insAC	GRCh38
NC_000011.9:g.113803375_113803376insAC , CM000673.1:g.113803375_113803376insAC	GRCh37
NC_000011.8:g.113308585_113308586insAC	NCBI36
NG_011483.1:g.32787_32788insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+195_538+196insAC MANE Select	ENSP00000260191.2:n.538+195_538+196insAC
ENST00000260191.7:c.538+195_538+196insAC	ENSP00000260191.2:n.538+195_538+196insAC
ENST00000260191.6:c.538+195_538+196insAC	ENSP00000260191.2:n.538+195_538+196insAC
ENST00000537778.5:c.505+195_505+196insAC	ENSP00000443118.1:n.505+195_505+196insAC
ENST00000543092.1:c.324+195_324+196insAC
NM_006028.4:c.538+195_538+196insAC	NP_006019.1:n.538+195_538+196insAC
XM_011543063.1:c.505+195_505+196insAC	XP_011541365.1:n.505+195_505+196insAC
XM_011543064.1:c.337+195_337+196insAC	XP_011541366.1:n.337+195_337+196insAC
XM_011543065.1:c.331+195_331+196insAC	XP_011541367.1:n.331+195_331+196insAC
XM_011543066.1:c.505+195_505+196insAC	XP_011541368.1:n.505+195_505+196insAC
NM_001363563.1:c.505+195_505+196insAC	NP_001350492.1:n.505+195_505+196insAC
XM_017018552.2:c.331+195_331+196insAC	XP_016874041.1:n.331+195_331+196insAC
XM_024448767.1:c.244+195_244+196insAC	XP_024304535.1:n.244+195_244+196insAC
XR_001748034.2:n.789+195_789+196insAC
NM_001363563.2:c.505+195_505+196insAC	NP_001350492.1:n.505+195_505+196insAC
NM_006028.5:c.538+195_538+196insAC MANE Select	NP_006019.1:n.538+195_538+196insAC