Canonical Allele Identifier: CA671969593

Gene: HTR3B

Linked Data

• dbSNP Id: rs1224982030
• MyVariant Identifiers: chr11:g.113781085_113781086insCCTCTT (hg19) ; chr11:g.113910363_113910364insCCTCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910374_113910379dup , CM000673.2:g.113910374_113910379dup	GRCh38
NC_000011.9:g.113781096_113781101dup , CM000673.1:g.113781096_113781101dup	GRCh37
NC_000011.8:g.113286306_113286311dup	NCBI36
NG_011483.1:g.10508_10513dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.213+919_213+924dup MANE Select	ENSP00000260191.2:n.213+919_213+924dup
ENST00000260191.7:c.213+919_213+924dup	ENSP00000260191.2:n.213+919_213+924dup
ENST00000260191.6:c.213+919_213+924dup	ENSP00000260191.2:n.213+919_213+924dup
ENST00000537778.5:c.180+919_180+924dup	ENSP00000443118.1:n.180+919_180+924dup
NM_006028.4:c.213+919_213+924dup	NP_006019.1:n.213+919_213+924dup
XM_011543063.1:c.180+919_180+924dup	XP_011541365.1:n.180+919_180+924dup
XM_011543064.1:c.12+11291_12+11296dup	XP_011541366.1:n.12+11291_12+11296dup
XM_011543066.1:c.180+919_180+924dup	XP_011541368.1:n.180+919_180+924dup
NM_001363563.1:c.180+919_180+924dup	NP_001350492.1:n.180+919_180+924dup
XM_024448767.1:c.-82+919_-82+924dup	XP_024304535.1:n.-82+919_-82+924dup
XR_001748034.2:n.464+919_464+924dup
NM_001363563.2:c.180+919_180+924dup	NP_001350492.1:n.180+919_180+924dup
NM_006028.5:c.213+919_213+924dup MANE Select	NP_006019.1:n.213+919_213+924dup