Canonical Allele Identifier: CA2089293957

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46860935G= , CM000675.2:g.46860935G=	GRCh38
NC_000013.10:g.47435070G= , CM000675.1:g.47435070G=	GRCh37
NC_000013.9:g.46333071G=	NCBI36
NG_013011.1:g.41100C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-25296C= MANE Select	ENSP00000437737.1:n.614-25296C=
ENST00000543956.5:c.125-25296C=	ENSP00000441861.2:n.125-25296C=
ENST00000378688.8:c.614-25296C=	ENSP00000367959.3:n.614-25296C=
ENST00000542664.3:c.614-25296C=	ENSP00000437737.1:n.614-25296C=
ENST00000543956.4:c.362-25296C=	ENSP00000441861.1:n.362-25296C=
NM_000621.4:c.614-25296C=	NP_000612.1:n.614-25296C=
NM_001165947.2:c.362-25296C=	NP_001159419.1:n.362-25296C=
NM_000621.5:c.614-25296C= MANE Select	NP_000612.1:n.614-25296C=
NM_001165947.5:c.125-25296C=	NP_001159419.2:n.125-25296C=
NM_001378924.1:c.614-25296C=	NP_001365853.1:n.614-25296C=