Canonical Allele Identifier: CA609569426

Gene: HTR2A

Linked Data

• dbSNP Id: rs1566298490
• gnomAD v2: 13-47409929-ATG-A
• gnomAD v3: 13-46835794-ATG-A
• gnomAD v4: 13-46835794-ATG-A
• MyVariant Identifiers: chr13:g.47409930_47409931del (hg19) ; chr13:g.46835795_46835796del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835798_46835799del , CM000675.2:g.46835798_46835799del	GRCh38
NC_000013.10:g.47409933_47409934del , CM000675.1:g.47409933_47409934del	GRCh37
NC_000013.9:g.46307934_46307935del	NCBI36
NG_013011.1:g.66239_66240del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-157_614-156del MANE Select	ENSP00000437737.1:n.614-157_614-156del
ENST00000543956.5:c.125-157_125-156del	ENSP00000441861.2:n.125-157_125-156del
ENST00000378688.8:c.614-157_614-156del	ENSP00000367959.3:n.614-157_614-156del
ENST00000542664.3:c.614-157_614-156del	ENSP00000437737.1:n.614-157_614-156del
ENST00000543956.4:c.362-157_362-156del	ENSP00000441861.1:n.362-157_362-156del
NM_000621.4:c.614-157_614-156del	NP_000612.1:n.614-157_614-156del
NM_001165947.2:c.362-157_362-156del	NP_001159419.1:n.362-157_362-156del
NM_000621.5:c.614-157_614-156del MANE Select	NP_000612.1:n.614-157_614-156del
NM_001165947.5:c.125-157_125-156del	NP_001159419.2:n.125-157_125-156del
NM_001378924.1:c.614-157_614-156del	NP_001365853.1:n.614-157_614-156del