Canonical Allele Identifier: CA2724883427

Gene: MTNR1B

Linked Data

• dbSNP Id: rs2136509151

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92972133A>C , CM000673.2:g.92972133A>C	GRCh38
NC_000011.9:g.92705299A>C , CM000673.1:g.92705299A>C	GRCh37
NC_000011.8:g.92344947A>C	NCBI36
NG_028160.1:g.7511A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257068.3:c.223+2185A>C MANE Select	ENSP00000257068.2:n.223+2185A>C
ENST00000257068.2:c.223+2185A>C	ENSP00000257068.2:n.223+2185A>C
ENST00000528076.1:c.165+2185A>C
ENST00000532482.1:c.224-328A>C	ENSP00000436101.1:n.224-328A>C
NM_005959.3:c.223+2185A>C	NP_005950.1:n.223+2185A>C
XM_011542839.1:c.223+2185A>C	XP_011541141.1:n.223+2185A>C
XM_011542839.2:c.223+2185A>C	XP_011541141.1:n.223+2185A>C
NM_005959.5:c.223+2185A>C MANE Select	NP_005950.1:n.223+2185A>C