Canonical Allele Identifier: CA2580593139

Gene: HCRTR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55276221G= , CM000668.2:g.55276221G=	GRCh38
NC_000006.11:g.55141019G= , CM000668.1:g.55141019G=	GRCh37
NC_000006.10:g.55248978G=	NCBI36
NG_012447.1:g.106949G=
NG_012447.2:g.174762G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.763-1159G= MANE Select	ENSP00000359899.3:n.763-1159G=
ENST00000370862.3:c.763-1159G=	ENSP00000359899.3:n.763-1159G=
ENST00000615358.4:c.763-1159G=	ENSP00000477548.1:n.763-1159G=
NM_001526.3:c.763-1159G=	NP_001517.2:n.763-1159G=
XM_011514542.1:c.568-1159G=	XP_011512844.1:n.568-1159G=
NM_001526.4:c.763-1159G=	NP_001517.2:n.763-1159G=
XM_017010798.1:c.763-1159G=	XP_016866287.1:n.763-1159G=
NM_001384272.1:c.763-1159G= MANE Select	NP_001371201.1:n.763-1159G=
NM_001526.5:c.763-1159G=	NP_001517.2:n.763-1159G=