Canonical Allele Identifier: CA2089308772

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892494G= , CM000675.2:g.46892494G=	GRCh38
NC_000013.10:g.47466629G= , CM000675.1:g.47466629G=	GRCh37
NC_000013.9:g.46364630G=	NCBI36
NG_013011.1:g.9541C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.509C= MANE Select	ENSP00000437737.1:p.Ser170=
ENST00000543956.5:c.20C=	ENSP00000441861.2:p.Ser7=
ENST00000378688.8:c.509C=	ENSP00000367959.3:p.Ser170=
ENST00000542664.3:c.509C=	ENSP00000437737.1:p.Ser170=
ENST00000543956.4:c.257C=	ENSP00000441861.1:p.Ser86=
NM_000621.4:c.509C=	NP_000612.1:p.Ser170=
NM_001165947.2:c.257C=	NP_001159419.1:p.Ser86=
NM_000621.5:c.509C= MANE Select	NP_000612.1:p.Ser170=
NM_001165947.5:c.20C=	NP_001159419.2:p.Ser7=
NM_001378924.1:c.509C=	NP_001365853.1:p.Ser170=