Canonical Allele Identifier: CA609929161

Gene: HTR2A

Linked Data

• dbSNP Id: rs1236402724
• gnomAD v2: 13-47409067-T-TTG
• gnomAD v4: 13-46834932-T-TTG
• MyVariant Identifiers: chr13:g.47409067_47409068insTG (hg19) ; chr13:g.46834932_46834933insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834932_46834933insTG , CM000675.2:g.46834932_46834933insTG	GRCh38
NC_000013.10:g.47409067_47409068insTG , CM000675.1:g.47409067_47409068insTG	GRCh37
NC_000013.9:g.46307068_46307069insTG	NCBI36
NG_013011.1:g.67102_67103insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1320_1321insCA MANE Select	ENSP00000437737.1:p.Asn441GlnfsTer9
ENST00000543956.5:c.831_832insCA	ENSP00000441861.2:p.Asn278GlnfsTer9
ENST00000378688.8:c.1320_1321insCA	ENSP00000367959.3:p.Asn441GlnfsTer9
ENST00000542664.3:c.1320_1321insCA	ENSP00000437737.1:p.Asn441GlnfsTer9
ENST00000543956.4:c.1068_1069insCA	ENSP00000441861.1:p.Asn357GlnfsTer9
NM_000621.4:c.1320_1321insCA	NP_000612.1:p.Asn441GlnfsTer9
NM_001165947.2:c.1068_1069insCA	NP_001159419.1:p.Asn357GlnfsTer9
NM_000621.5:c.1320_1321insCA MANE Select	NP_000612.1:p.Asn441GlnfsTer9
NM_001165947.5:c.831_832insCA	NP_001159419.2:p.Asn278GlnfsTer9
NM_001378924.1:c.1320_1321insCA	NP_001365853.1:p.Asn441GlnfsTer9