Canonical Allele Identifier: CA609564303

Gene: HTR2A

Linked Data

• dbSNP Id: rs1311835389
• gnomAD v2: 13-47419788-AAAAAAAAG-A
• gnomAD v3: 13-46845653-AAAAAAAAG-A
• gnomAD v4: 13-46845653-AAAAAAAAG-A
• MyVariant Identifiers: chr13:g.47419789_47419796del (hg19) ; chr13:g.46845654_46845661del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845663_46845670del , CM000675.2:g.46845663_46845670del	GRCh38
NC_000013.10:g.47419798_47419805del , CM000675.1:g.47419798_47419805del	GRCh37
NC_000013.9:g.46317799_46317806del	NCBI36
NG_013011.1:g.56374_56381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-10022_614-10015del MANE Select	ENSP00000437737.1:n.614-10022_614-10015del
ENST00000543956.5:c.125-10022_125-10015del	ENSP00000441861.2:n.125-10022_125-10015del
ENST00000378688.8:c.614-10022_614-10015del	ENSP00000367959.3:n.614-10022_614-10015del
ENST00000542664.3:c.614-10022_614-10015del	ENSP00000437737.1:n.614-10022_614-10015del
ENST00000543956.4:c.362-10022_362-10015del	ENSP00000441861.1:n.362-10022_362-10015del
NM_000621.4:c.614-10022_614-10015del	NP_000612.1:n.614-10022_614-10015del
NM_001165947.2:c.362-10022_362-10015del	NP_001159419.1:n.362-10022_362-10015del
NM_000621.5:c.614-10022_614-10015del MANE Select	NP_000612.1:n.614-10022_614-10015del
NM_001165947.5:c.125-10022_125-10015del	NP_001159419.2:n.125-10022_125-10015del
NM_001378924.1:c.614-10022_614-10015del	NP_001365853.1:n.614-10022_614-10015del