Canonical Allele Identifier: CA955693767

Gene: HTR2A

Linked Data

• dbSNP Id: rs1657073037
• gnomAD v3: 13-46860979-G-GAT
• gnomAD v4: 13-46860979-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46860986_46860987dup , CM000675.2:g.46860986_46860987dup	GRCh38
NC_000013.10:g.47435121_47435122dup , CM000675.1:g.47435121_47435122dup	GRCh37
NC_000013.9:g.46333122_46333123dup	NCBI36
NG_013011.1:g.41054_41055dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-25342_614-25341dup MANE Select	ENSP00000437737.1:n.614-25342_614-25341du...
ENST00000543956.5:c.125-25342_125-25341dup	ENSP00000441861.2:n.125-25342_125-25341du...
ENST00000378688.8:c.614-25342_614-25341dup	ENSP00000367959.3:n.614-25342_614-25341du...
ENST00000542664.3:c.614-25342_614-25341dup	ENSP00000437737.1:n.614-25342_614-25341du...
ENST00000543956.4:c.362-25342_362-25341dup	ENSP00000441861.1:n.362-25342_362-25341du...
NM_000621.4:c.614-25342_614-25341dup	NP_000612.1:n.614-25342_614-25341dup
NM_001165947.2:c.362-25342_362-25341dup	NP_001159419.1:n.362-25342_362-25341dup
NM_000621.5:c.614-25342_614-25341dup MANE Select	NP_000612.1:n.614-25342_614-25341dup
NM_001165947.5:c.125-25342_125-25341dup	NP_001159419.2:n.125-25342_125-25341dup
NM_001378924.1:c.614-25342_614-25341dup	NP_001365853.1:n.614-25342_614-25341dup