Canonical Allele Identifier: CA609564304

Gene: HTR2A

Linked Data

• dbSNP Id: rs1566301809
• gnomAD v2: 13-47419788-A-AG
• gnomAD v3: 13-46845653-A-AG
• gnomAD v4: 13-46845653-A-AG
• MyVariant Identifiers: chr13:g.47419789_47419796delinsGAAAAAAAG (hg19) ; chr13:g.46845654_46845661delinsGAAAAAAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845653_46845654insG , CM000675.2:g.46845653_46845654insG	GRCh38
NC_000013.10:g.47419788_47419789insG , CM000675.1:g.47419788_47419789insG	GRCh37
NC_000013.9:g.46317789_46317790insG	NCBI36
NG_013011.1:g.56381_56382insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-10015_614-10014insC MANE Select	ENSP00000437737.1:n.614-10015_614-10014insC
ENST00000543956.5:c.125-10015_125-10014insC	ENSP00000441861.2:n.125-10015_125-10014insC
ENST00000378688.8:c.614-10015_614-10014insC	ENSP00000367959.3:n.614-10015_614-10014insC
ENST00000542664.3:c.614-10015_614-10014insC	ENSP00000437737.1:n.614-10015_614-10014insC
ENST00000543956.4:c.362-10015_362-10014insC	ENSP00000441861.1:n.362-10015_362-10014insC
NM_000621.4:c.614-10015_614-10014insC	NP_000612.1:n.614-10015_614-10014insC
NM_001165947.2:c.362-10015_362-10014insC	NP_001159419.1:n.362-10015_362-10014insC
NM_000621.5:c.614-10015_614-10014insC MANE Select	NP_000612.1:n.614-10015_614-10014insC
NM_001165947.5:c.125-10015_125-10014insC	NP_001159419.2:n.125-10015_125-10014insC
NM_001378924.1:c.614-10015_614-10014insC	NP_001365853.1:n.614-10015_614-10014insC