Canonical Allele Identifier: CA2089308781

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892508G= , CM000675.2:g.46892508G=	GRCh38
NC_000013.10:g.47466643G= , CM000675.1:g.47466643G=	GRCh37
NC_000013.9:g.46364644G=	NCBI36
NG_013011.1:g.9527C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.495C= MANE Select	ENSP00000437737.1:p.His165=
ENST00000543956.5:c.6C=	ENSP00000441861.2:p.His2=
ENST00000378688.8:c.495C=	ENSP00000367959.3:p.His165=
ENST00000542664.3:c.495C=	ENSP00000437737.1:p.His165=
ENST00000543956.4:c.243C=	ENSP00000441861.1:p.His81=
NM_000621.4:c.495C=	NP_000612.1:p.His165=
NM_001165947.2:c.243C=	NP_001159419.1:p.His81=
NM_000621.5:c.495C= MANE Select	NP_000612.1:p.His165=
NM_001165947.5:c.6C=	NP_001159419.2:p.His2=
NM_001378924.1:c.495C=	NP_001365853.1:p.His165=