Canonical Allele Identifier: CA2452892592

Gene: HTR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114849062T= , CM000685.2:g.114849062T=	GRCh38
NC_000023.10:g.114083625T= , CM000685.1:g.114083625T=	GRCh37
NC_000023.9:g.113989881T=	NCBI36
NG_012082.2:g.269978T=
NG_012082.3:g.269978T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276198.6:c.550+859T= MANE Select	ENSP00000276198.1:n.550+859T=
ENST00000276198.5:c.550+859T=	ENSP00000276198.1:n.550+859T=
ENST00000371950.3:c.455+954T=	ENSP00000361018.3:n.455+954T=
ENST00000371951.5:c.550+859T=	ENSP00000361019.1:n.550+859T=
NM_000868.3:c.550+859T=	NP_000859.1:n.550+859T=
NM_001256760.2:c.550+859T=	NP_001243689.1:n.550+859T=
NM_001256761.2:c.455+954T=	NP_001243690.1:n.455+954T=
NM_000868.4:c.550+859T= MANE Select	NP_000859.2:n.550+859T=
NM_001256760.3:c.550+859T=	NP_001243689.2:n.550+859T=
NM_001256761.3:c.455+954T=	NP_001243690.2:n.455+954T=