Canonical Allele Identifier: CA1991753333

Gene: MTNR1B

Linked Data

• dbSNP Id: rs1857937595

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92972181A>T , CM000673.2:g.92972181A>T	GRCh38
NC_000011.9:g.92705347A>T , CM000673.1:g.92705347A>T	GRCh37
NC_000011.8:g.92344995A>T	NCBI36
NG_028160.1:g.7559A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257068.3:c.223+2233A>T MANE Select	ENSP00000257068.2:n.223+2233A>T
ENST00000257068.2:c.223+2233A>T	ENSP00000257068.2:n.223+2233A>T
ENST00000528076.1:c.165+2233A>T
ENST00000532482.1:c.224-280A>T	ENSP00000436101.1:n.224-280A>T
NM_005959.3:c.223+2233A>T	NP_005950.1:n.223+2233A>T
XM_011542839.1:c.223+2233A>T	XP_011541141.1:n.223+2233A>T
XM_011542839.2:c.223+2233A>T	XP_011541141.1:n.223+2233A>T
NM_005959.5:c.223+2233A>T MANE Select	NP_005950.1:n.223+2233A>T