Canonical Allele Identifier: CA2089296707

Gene: HTR2A

Linked Data

• dbSNP Id: rs1950818666

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46866422_46866434del , CM000675.2:g.46866422_46866434del	GRCh38
NC_000013.10:g.47440557_47440569del , CM000675.1:g.47440557_47440569del	GRCh37
NC_000013.9:g.46338558_46338570del	NCBI36
NG_013011.1:g.35602_35614del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.613+25957_613+25969del MANE Select	ENSP00000437737.1:n.613+25957_613+25969de...
ENST00000543956.5:c.124+25957_124+25969del	ENSP00000441861.2:n.124+25957_124+25969de...
ENST00000378688.8:c.613+25957_613+25969del	ENSP00000367959.3:n.613+25957_613+25969de...
ENST00000542664.3:c.613+25957_613+25969del	ENSP00000437737.1:n.613+25957_613+25969de...
ENST00000543956.4:c.361+25957_361+25969del	ENSP00000441861.1:n.361+25957_361+25969de...
NM_000621.4:c.613+25957_613+25969del	NP_000612.1:n.613+25957_613+25969del
NM_001165947.2:c.361+25957_361+25969del	NP_001159419.1:n.361+25957_361+25969del
NM_000621.5:c.613+25957_613+25969del MANE Select	NP_000612.1:n.613+25957_613+25969del
NM_001165947.5:c.124+25957_124+25969del	NP_001159419.2:n.124+25957_124+25969del
NM_001378924.1:c.613+25957_613+25969del	NP_001365853.1:n.613+25957_613+25969del