Canonical Allele Identifier: CA955688432

Gene: HTR2A

Linked Data

• dbSNP Id: rs1950825752

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46867348T>A , CM000675.2:g.46867348T>A	GRCh38
NC_000013.10:g.47441483T>A , CM000675.1:g.47441483T>A	GRCh37
NC_000013.9:g.46339484T>A	NCBI36
NG_013011.1:g.34687A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+25042A>T MANE Select	ENSP00000437737.1:n.613+25042A>T
ENST00000543956.5:c.124+25042A>T	ENSP00000441861.2:n.124+25042A>T
ENST00000378688.8:c.613+25042A>T	ENSP00000367959.3:n.613+25042A>T
ENST00000542664.3:c.613+25042A>T	ENSP00000437737.1:n.613+25042A>T
ENST00000543956.4:c.361+25042A>T	ENSP00000441861.1:n.361+25042A>T
NM_000621.4:c.613+25042A>T	NP_000612.1:n.613+25042A>T
NM_001165947.2:c.361+25042A>T	NP_001159419.1:n.361+25042A>T
NM_000621.5:c.613+25042A>T MANE Select	NP_000612.1:n.613+25042A>T
NM_001165947.5:c.124+25042A>T	NP_001159419.2:n.124+25042A>T
NM_001378924.1:c.613+25042A>T	NP_001365853.1:n.613+25042A>T