Canonical Allele Identifier: CA13467238

Gene: MTNR1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92975544C>G , CM000673.2:g.92975544C>G	GRCh38
NC_000011.9:g.92708710C>G , CM000673.1:g.92708710C>G	GRCh37
NC_000011.8:g.92348358C>G	NCBI36
NG_028160.1:g.10922C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257068.3:c.223+5596C>G MANE Select	ENSP00000257068.2:n.223+5596C>G
ENST00000257068.2:c.223+5596C>G	ENSP00000257068.2:n.223+5596C>G
ENST00000528076.1:c.165+5596C>G
ENST00000532482.1:c.354+2953C>G	ENSP00000436101.1:n.354+2953C>G
NM_005959.3:c.223+5596C>G	NP_005950.1:n.223+5596C>G
XM_011542839.1:c.223+5596C>G	XP_011541141.1:n.223+5596C>G
XM_011542839.2:c.223+5596C>G	XP_011541141.1:n.223+5596C>G
NM_005959.5:c.223+5596C>G MANE Select	NP_005950.1:n.223+5596C>G