Canonical Allele Identifier: CA2452862047

Gene: HTR2C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114765807T= , CM000685.2:g.114765807T=	GRCh38
NG_012082.2:g.186723T=
NG_012082.3:g.186723T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276198.6:c.349+34200T= MANE Select	ENSP00000276198.1:n.349+34200T=
ENST00000276198.5:c.349+34200T=	ENSP00000276198.1:n.349+34200T=
ENST00000371950.3:c.349+34200T=	ENSP00000361018.3:n.349+34200T=
ENST00000371951.5:c.349+34200T=	ENSP00000361019.1:n.349+34200T=
NM_000868.3:c.349+34200T=	NP_000859.1:n.349+34200T=
NM_001256760.2:c.349+34200T=	NP_001243689.1:n.349+34200T=
NM_001256761.2:c.349+34200T=	NP_001243690.1:n.349+34200T=
XR_944300.1:n.208+23536A=
XR_944301.1:n.208+23536A=
XR_001755943.1:n.208+23536A=
NM_000868.4:c.349+34200T= MANE Select	NP_000859.2:n.349+34200T=
NM_001256760.3:c.349+34200T=	NP_001243689.2:n.349+34200T=
NM_001256761.3:c.349+34200T=	NP_001243690.2:n.349+34200T=