Canonical Allele Identifier: CA2452910326

Gene: HTR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114903634G= , CM000685.2:g.114903634G=	GRCh38
NC_000023.10:g.114138197G= , CM000685.1:g.114138197G=	GRCh37
NC_000023.9:g.114044453G=	NCBI36
NG_012082.2:g.324550G=
NG_012082.3:g.324550G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000276198.6:c.551-2955G= MANE Select	ENSP00000276198.1:n.551-2955G=
ENST00000276198.5:c.551-2955G=	ENSP00000276198.1:n.551-2955G=
ENST00000371950.3:c.456-2955G=	ENSP00000361018.3:n.456-2955G=
ENST00000371951.5:c.551-2955G=	ENSP00000361019.1:n.551-2955G=
NM_000868.3:c.551-2955G=	NP_000859.1:n.551-2955G=
NM_001256760.2:c.551-2955G=	NP_001243689.1:n.551-2955G=
NM_001256761.2:c.456-2955G=	NP_001243690.1:n.456-2955G=
NM_000868.4:c.551-2955G= MANE Select	NP_000859.2:n.551-2955G=
NM_001256760.3:c.551-2955G=	NP_001243689.2:n.551-2955G=
NM_001256761.3:c.456-2955G=	NP_001243690.2:n.456-2955G=