Canonical Allele Identifier: CA955687060

Gene: HTR2A

Linked Data

• dbSNP Id: rs1876438623
• gnomAD v3: 13-46835916-ATAT-A
• gnomAD v4: 13-46835916-ATAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835920_46835922del , CM000675.2:g.46835920_46835922del	GRCh38
NC_000013.10:g.47410055_47410057del , CM000675.1:g.47410055_47410057del	GRCh37
NC_000013.9:g.46308056_46308058del	NCBI36
NG_013011.1:g.66116_66118del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-280_614-278del MANE Select	ENSP00000437737.1:n.614-280_614-278del
ENST00000543956.5:c.125-280_125-278del	ENSP00000441861.2:n.125-280_125-278del
ENST00000378688.8:c.614-280_614-278del	ENSP00000367959.3:n.614-280_614-278del
ENST00000542664.3:c.614-280_614-278del	ENSP00000437737.1:n.614-280_614-278del
ENST00000543956.4:c.362-280_362-278del	ENSP00000441861.1:n.362-280_362-278del
NM_000621.4:c.614-280_614-278del	NP_000612.1:n.614-280_614-278del
NM_001165947.2:c.362-280_362-278del	NP_001159419.1:n.362-280_362-278del
NM_000621.5:c.614-280_614-278del MANE Select	NP_000612.1:n.614-280_614-278del
NM_001165947.5:c.125-280_125-278del	NP_001159419.2:n.125-280_125-278del
NM_001378924.1:c.614-280_614-278del	NP_001365853.1:n.614-280_614-278del