Canonical Allele Identifier: CA2089284488

Gene: HTR2A

Linked Data

• dbSNP Id: rs1950572967
• gnomAD v3: 13-46837891-CT-C
• gnomAD v4: 13-46837891-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46837893del , CM000675.2:g.46837893del	GRCh38
NC_000013.10:g.47412028del , CM000675.1:g.47412028del	GRCh37
NC_000013.9:g.46310029del	NCBI36
NG_013011.1:g.64143del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-2253del MANE Select	ENSP00000437737.1:n.614-2253del
ENST00000543956.5:c.125-2253del	ENSP00000441861.2:n.125-2253del
ENST00000378688.8:c.614-2253del	ENSP00000367959.3:n.614-2253del
ENST00000542664.3:c.614-2253del	ENSP00000437737.1:n.614-2253del
ENST00000543956.4:c.362-2253del	ENSP00000441861.1:n.362-2253del
NM_000621.4:c.614-2253del	NP_000612.1:n.614-2253del
NM_001165947.2:c.362-2253del	NP_001159419.1:n.362-2253del
NM_000621.5:c.614-2253del MANE Select	NP_000612.1:n.614-2253del
NM_001165947.5:c.125-2253del	NP_001159419.2:n.125-2253del
NM_001378924.1:c.614-2253del	NP_001365853.1:n.614-2253del