Canonical Allele Identifier: CA2089297078

Gene: HTR2A

Linked Data

• dbSNP Id: rs1950824613
• gnomAD v3: 13-46867201-AAGTC-A
• gnomAD v4: 13-46867201-AAGTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46867202_46867205del , CM000675.2:g.46867202_46867205del	GRCh38
NC_000013.10:g.47441337_47441340del , CM000675.1:g.47441337_47441340del	GRCh37
NC_000013.9:g.46339338_46339341del	NCBI36
NG_013011.1:g.34830_34833del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+25185_613+25188del MANE Select	ENSP00000437737.1:n.613+25185_613+25188del
ENST00000543956.5:c.124+25185_124+25188del	ENSP00000441861.2:n.124+25185_124+25188del
ENST00000378688.8:c.613+25185_613+25188del	ENSP00000367959.3:n.613+25185_613+25188del
ENST00000542664.3:c.613+25185_613+25188del	ENSP00000437737.1:n.613+25185_613+25188del
ENST00000543956.4:c.361+25185_361+25188del	ENSP00000441861.1:n.361+25185_361+25188del
NM_000621.4:c.613+25185_613+25188del	NP_000612.1:n.613+25185_613+25188del
NM_001165947.2:c.361+25185_361+25188del	NP_001159419.1:n.361+25185_361+25188del
NM_000621.5:c.613+25185_613+25188del MANE Select	NP_000612.1:n.613+25185_613+25188del
NM_001165947.5:c.124+25185_124+25188del	NP_001159419.2:n.124+25185_124+25188del
NM_001378924.1:c.613+25185_613+25188del	NP_001365853.1:n.613+25185_613+25188del