Canonical Allele Identifier: CA955693399

Gene: HTR2A

Linked Data

• dbSNP Id: rs1950761022
• gnomAD v3: 13-46859086-T-C
• gnomAD v4: 13-46859086-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46859086T>C , CM000675.2:g.46859086T>C	GRCh38
NC_000013.10:g.47433221T>C , CM000675.1:g.47433221T>C	GRCh37
NC_000013.9:g.46331222T>C	NCBI36
NG_013011.1:g.42949A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-23447A>G MANE Select	ENSP00000437737.1:n.614-23447A>G
ENST00000543956.5:c.125-23447A>G	ENSP00000441861.2:n.125-23447A>G
ENST00000378688.8:c.614-23447A>G	ENSP00000367959.3:n.614-23447A>G
ENST00000542664.3:c.614-23447A>G	ENSP00000437737.1:n.614-23447A>G
ENST00000543956.4:c.362-23447A>G	ENSP00000441861.1:n.362-23447A>G
NM_000621.4:c.614-23447A>G	NP_000612.1:n.614-23447A>G
NM_001165947.2:c.362-23447A>G	NP_001159419.1:n.362-23447A>G
NM_000621.5:c.614-23447A>G MANE Select	NP_000612.1:n.614-23447A>G
NM_001165947.5:c.125-23447A>G	NP_001159419.2:n.125-23447A>G
NM_001378924.1:c.614-23447A>G	NP_001365853.1:n.614-23447A>G