Canonical Allele Identifier: CA1991753232

Gene: MTNR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92971967A= , CM000673.2:g.92971967A=	GRCh38
NC_000011.9:g.92705133A= , CM000673.1:g.92705133A=	GRCh37
NC_000011.8:g.92344781A=	NCBI36
NG_028160.1:g.7345A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257068.3:c.223+2019A= MANE Select	ENSP00000257068.2:n.223+2019A=
ENST00000257068.2:c.223+2019A=	ENSP00000257068.2:n.223+2019A=
ENST00000528076.1:c.165+2019A=
ENST00000532482.1:c.224-494A=	ENSP00000436101.1:n.224-494A=
NM_005959.3:c.223+2019A=	NP_005950.1:n.223+2019A=
XM_011542839.1:c.223+2019A=	XP_011541141.1:n.223+2019A=
XM_011542839.2:c.223+2019A=	XP_011541141.1:n.223+2019A=
NM_005959.5:c.223+2019A= MANE Select	NP_005950.1:n.223+2019A=