Canonical Allele Identifier: CA698569499

Gene: HTR2A

Linked Data

• dbSNP Id: rs1371064169
• gnomAD v3: 13-46861209-AAGG-A
• gnomAD v4: 13-46861209-AAGG-A
• MyVariant Identifiers: chr13:g.47435345_47435347del (hg19) ; chr13:g.46861210_46861212del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46861212_46861214del , CM000675.2:g.46861212_46861214del	GRCh38
NC_000013.10:g.47435347_47435349del , CM000675.1:g.47435347_47435349del	GRCh37
NC_000013.9:g.46333348_46333350del	NCBI36
NG_013011.1:g.40823_40825del

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-25573_614-25571del MANE Select	ENSP00000437737.1:n.614-25573_614-25571de...
ENST00000543956.5:c.125-25573_125-25571del	ENSP00000441861.2:n.125-25573_125-25571de...
ENST00000378688.8:c.614-25573_614-25571del	ENSP00000367959.3:n.614-25573_614-25571de...
ENST00000542664.3:c.614-25573_614-25571del	ENSP00000437737.1:n.614-25573_614-25571de...
ENST00000543956.4:c.362-25573_362-25571del	ENSP00000441861.1:n.362-25573_362-25571de...
NM_000621.4:c.614-25573_614-25571del	NP_000612.1:n.614-25573_614-25571del
NM_001165947.2:c.362-25573_362-25571del	NP_001159419.1:n.362-25573_362-25571del
NM_000621.5:c.614-25573_614-25571del MANE Select	NP_000612.1:n.614-25573_614-25571del
NM_001165947.5:c.125-25573_125-25571del	NP_001159419.2:n.125-25573_125-25571del
NM_001378924.1:c.614-25573_614-25571del	NP_001365853.1:n.614-25573_614-25571del