Canonical Allele Identifier: CA1991753260

Gene: MTNR1B

Linked Data

• dbSNP Id: rs1857934660

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92972034A>G , CM000673.2:g.92972034A>G	GRCh38
NC_000011.9:g.92705200A>G , CM000673.1:g.92705200A>G	GRCh37
NC_000011.8:g.92344848A>G	NCBI36
NG_028160.1:g.7412A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257068.3:c.223+2086A>G MANE Select	ENSP00000257068.2:n.223+2086A>G
ENST00000257068.2:c.223+2086A>G	ENSP00000257068.2:n.223+2086A>G
ENST00000528076.1:c.165+2086A>G
ENST00000532482.1:c.224-427A>G	ENSP00000436101.1:n.224-427A>G
NM_005959.3:c.223+2086A>G	NP_005950.1:n.223+2086A>G
XM_011542839.1:c.223+2086A>G	XP_011541141.1:n.223+2086A>G
XM_011542839.2:c.223+2086A>G	XP_011541141.1:n.223+2086A>G
NM_005959.5:c.223+2086A>G MANE Select	NP_005950.1:n.223+2086A>G