Canonical Allele Identifier: CA2452800065

Gene: HTR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114590222G= , CM000685.2:g.114590222G=	GRCh38
NG_012082.2:g.11138G=
NG_012082.3:g.11138G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000868.4:c.-147+5563G= MANE Select	NP_000859.2:n.-147+5563G=
ENST00000276198.6:c.-147+5563G= MANE Select	ENSP00000276198.1:n.-147+5563G=
NM_000868.3:c.-147+5563G=	NP_000859.1:n.-147+5563G=
NM_001256760.2:c.-238+5563G=	NP_001243689.1:n.-238+5563G=
NM_001256760.3:c.-238+5563G=	NP_001243689.2:n.-238+5563G=
NM_001256761.2:c.-147+5563G=	NP_001243690.1:n.-147+5563G=
NM_001256761.3:c.-147+5563G=	NP_001243690.2:n.-147+5563G=
ENST00000276198.5:c.-147+5563G=	ENSP00000276198.1:n.-147+5563G=
ENST00000371950.3:c.-147+5563G=	ENSP00000361018.3:n.-147+5563G=
ENST00000371951.5:c.-238+5563G=	ENSP00000361019.1:n.-238+5563G=