Canonical Allele Identifier: CA1991753328

Gene: MTNR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92972174G= , CM000673.2:g.92972174G=	GRCh38
NC_000011.9:g.92705340G= , CM000673.1:g.92705340G=	GRCh37
NC_000011.8:g.92344988G=	NCBI36
NG_028160.1:g.7552G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257068.3:c.223+2226G= MANE Select	ENSP00000257068.2:n.223+2226G=
ENST00000257068.2:c.223+2226G=	ENSP00000257068.2:n.223+2226G=
ENST00000528076.1:c.165+2226G=
ENST00000532482.1:c.224-287G=	ENSP00000436101.1:n.224-287G=
NM_005959.3:c.223+2226G=	NP_005950.1:n.223+2226G=
XM_011542839.1:c.223+2226G=	XP_011541141.1:n.223+2226G=
XM_011542839.2:c.223+2226G=	XP_011541141.1:n.223+2226G=
NM_005959.5:c.223+2226G= MANE Select	NP_005950.1:n.223+2226G=