Canonical Allele Identifier: CA1991753262

Gene: MTNR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92972043C= , CM000673.2:g.92972043C=	GRCh38
NC_000011.9:g.92705209C= , CM000673.1:g.92705209C=	GRCh37
NC_000011.8:g.92344857C=	NCBI36
NG_028160.1:g.7421C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257068.3:c.223+2095C= MANE Select	ENSP00000257068.2:n.223+2095C=
ENST00000257068.2:c.223+2095C=	ENSP00000257068.2:n.223+2095C=
ENST00000528076.1:c.165+2095C=
ENST00000532482.1:c.224-418C=	ENSP00000436101.1:n.224-418C=
NM_005959.3:c.223+2095C=	NP_005950.1:n.223+2095C=
XM_011542839.1:c.223+2095C=	XP_011541141.1:n.223+2095C=
XM_011542839.2:c.223+2095C=	XP_011541141.1:n.223+2095C=
NM_005959.5:c.223+2095C= MANE Select	NP_005950.1:n.223+2095C=