Canonical Allele Identifier: CA13392559

Gene: MTNR1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92980341G>T , CM000673.2:g.92980341G>T	GRCh38
NC_000011.9:g.92713507G>T , CM000673.1:g.92713507G>T	GRCh37
NC_000011.8:g.92353155G>T	NCBI36
NG_028160.1:g.15719G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257068.3:c.224-1106G>T MANE Select	ENSP00000257068.2:n.224-1106G>T
ENST00000257068.2:c.224-1106G>T	ENSP00000257068.2:n.224-1106G>T
ENST00000528076.1:c.166-4466G>T
ENST00000532482.1:c.355-1106G>T	ENSP00000436101.1:n.355-1106G>T
NM_005959.3:c.224-1106G>T	NP_005950.1:n.224-1106G>T
XM_011542839.1:c.224-1106G>T	XP_011541141.1:n.224-1106G>T
XM_011542839.2:c.224-1106G>T	XP_011541141.1:n.224-1106G>T
XM_017017777.1:c.98-1106G>T	XP_016873266.1:n.98-1106G>T
NM_005959.5:c.224-1106G>T MANE Select	NP_005950.1:n.224-1106G>T