Canonical Allele Identifier: CA955687557

Gene: HTR2A

Linked Data

• dbSNP Id: rs1950571551
• gnomAD v3: 13-46837765-TGGCCA-T
• gnomAD v4: 13-46837765-TGGCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46837768_46837772del , CM000675.2:g.46837768_46837772del	GRCh38
NC_000013.10:g.47411903_47411907del , CM000675.1:g.47411903_47411907del	GRCh37
NC_000013.9:g.46309904_46309908del	NCBI36
NG_013011.1:g.64265_64269del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-2131_614-2127del MANE Select	ENSP00000437737.1:n.614-2131_614-2127del
ENST00000543956.5:c.125-2131_125-2127del	ENSP00000441861.2:n.125-2131_125-2127del
ENST00000378688.8:c.614-2131_614-2127del	ENSP00000367959.3:n.614-2131_614-2127del
ENST00000542664.3:c.614-2131_614-2127del	ENSP00000437737.1:n.614-2131_614-2127del
ENST00000543956.4:c.362-2131_362-2127del	ENSP00000441861.1:n.362-2131_362-2127del
NM_000621.4:c.614-2131_614-2127del	NP_000612.1:n.614-2131_614-2127del
NM_001165947.2:c.362-2131_362-2127del	NP_001159419.1:n.362-2131_362-2127del
NM_000621.5:c.614-2131_614-2127del MANE Select	NP_000612.1:n.614-2131_614-2127del
NM_001165947.5:c.125-2131_125-2127del	NP_001159419.2:n.125-2131_125-2127del
NM_001378924.1:c.614-2131_614-2127del	NP_001365853.1:n.614-2131_614-2127del