Canonical Allele Identifier: CA2089283422

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835065C= , CM000675.2:g.46835065C=	GRCh38
NC_000013.10:g.47409200C= , CM000675.1:g.47409200C=	GRCh37
NC_000013.9:g.46307201C=	NCBI36
NG_013011.1:g.66970G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1188G= MANE Select	ENSP00000437737.1:p.Gln396=
ENST00000543956.5:c.699G=	ENSP00000441861.2:p.Gln233=
ENST00000378688.8:c.1188G=	ENSP00000367959.3:p.Gln396=
ENST00000542664.3:c.1188G=	ENSP00000437737.1:p.Gln396=
ENST00000543956.4:c.936G=	ENSP00000441861.1:p.Gln312=
NM_000621.4:c.1188G=	NP_000612.1:p.Gln396=
NM_001165947.2:c.936G=	NP_001159419.1:p.Gln312=
NM_000621.5:c.1188G= MANE Select	NP_000612.1:p.Gln396=
NM_001165947.5:c.699G=	NP_001159419.2:p.Gln233=
NM_001378924.1:c.1188G=	NP_001365853.1:p.Gln396=