Canonical Allele Identifier: CA2452910330

Gene: HTR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114903671T= , CM000685.2:g.114903671T=	GRCh38
NC_000023.10:g.114138234T= , CM000685.1:g.114138234T=	GRCh37
NC_000023.9:g.114044490T=	NCBI36
NG_012082.2:g.324587T=
NG_012082.3:g.324587T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000276198.6:c.551-2918T= MANE Select	ENSP00000276198.1:n.551-2918T=
ENST00000276198.5:c.551-2918T=	ENSP00000276198.1:n.551-2918T=
ENST00000371950.3:c.456-2918T=	ENSP00000361018.3:n.456-2918T=
ENST00000371951.5:c.551-2918T=	ENSP00000361019.1:n.551-2918T=
NM_000868.3:c.551-2918T=	NP_000859.1:n.551-2918T=
NM_001256760.2:c.551-2918T=	NP_001243689.1:n.551-2918T=
NM_001256761.2:c.456-2918T=	NP_001243690.1:n.456-2918T=
NM_000868.4:c.551-2918T= MANE Select	NP_000859.2:n.551-2918T=
NM_001256760.3:c.551-2918T=	NP_001243689.2:n.551-2918T=
NM_001256761.3:c.456-2918T=	NP_001243690.2:n.456-2918T=