Canonical Allele Identifier: CA249242920

Gene: HTR2A

Linked Data

• dbSNP Id: rs35805696
• MyVariant Identifiers: chr13:g.47440913_47440914insT (hg19) ; chr13:g.46866778_46866779insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46866778_46866779insT , CM000675.2:g.46866778_46866779insT	GRCh38
NC_000013.10:g.47440913_47440914insT , CM000675.1:g.47440913_47440914insT	GRCh37
NC_000013.9:g.46338914_46338915insT	NCBI36
NG_013011.1:g.35256_35257insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+25611_613+25612insA MANE Select	ENSP00000437737.1:n.613+25611_613+25612insA
ENST00000543956.5:c.124+25611_124+25612insA	ENSP00000441861.2:n.124+25611_124+25612insA
ENST00000378688.8:c.613+25611_613+25612insA	ENSP00000367959.3:n.613+25611_613+25612insA
ENST00000542664.3:c.613+25611_613+25612insA	ENSP00000437737.1:n.613+25611_613+25612insA
ENST00000543956.4:c.361+25611_361+25612insA	ENSP00000441861.1:n.361+25611_361+25612insA
NM_000621.4:c.613+25611_613+25612insA	NP_000612.1:n.613+25611_613+25612insA
NM_001165947.2:c.361+25611_361+25612insA	NP_001159419.1:n.361+25611_361+25612insA
NM_000621.5:c.613+25611_613+25612insA MANE Select	NP_000612.1:n.613+25611_613+25612insA
NM_001165947.5:c.124+25611_124+25612insA	NP_001159419.2:n.124+25611_124+25612insA
NM_001378924.1:c.613+25611_613+25612insA	NP_001365853.1:n.613+25611_613+25612insA