Canonical Allele Identifier: CA2089308919

Gene: HTR2A

Linked Data

• dbSNP Id: rs1951063297

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892654T>A , CM000675.2:g.46892654T>A	GRCh38
NC_000013.10:g.47466789T>A , CM000675.1:g.47466789T>A	GRCh37
NC_000013.9:g.46364790T>A	NCBI36
NG_013011.1:g.9381A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.413-64A>T MANE Select	ENSP00000437737.1:n.413-64A>T
ENST00000543956.5:c.-77-64A>T	ENSP00000441861.2:n.-77-64A>T
ENST00000378688.8:c.413-64A>T	ENSP00000367959.3:n.413-64A>T
ENST00000542664.3:c.413-64A>T	ENSP00000437737.1:n.413-64A>T
ENST00000543956.4:c.161-64A>T	ENSP00000441861.1:n.161-64A>T
NM_000621.4:c.413-64A>T	NP_000612.1:n.413-64A>T
NM_001165947.2:c.161-64A>T	NP_001159419.1:n.161-64A>T
NM_000621.5:c.413-64A>T MANE Select	NP_000612.1:n.413-64A>T
NM_001165947.5:c.-77-64A>T	NP_001159419.2:n.-77-64A>T
NM_001378924.1:c.413-64A>T	NP_001365853.1:n.413-64A>T