Canonical Allele Identifier: CA226956155

Gene: MTNR1B

Linked Data

• dbSNP Id: rs907796874
• gnomAD v3: 11-92972174-G-A
• gnomAD v4: 11-92972174-G-A
• MyVariant Identifiers: chr11:g.92705340G>A (hg19) ; chr11:g.92972174G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92972174G>A , CM000673.2:g.92972174G>A	GRCh38
NC_000011.9:g.92705340G>A , CM000673.1:g.92705340G>A	GRCh37
NC_000011.8:g.92344988G>A	NCBI36
NG_028160.1:g.7552G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257068.3:c.223+2226G>A MANE Select	ENSP00000257068.2:n.223+2226G>A
ENST00000257068.2:c.223+2226G>A	ENSP00000257068.2:n.223+2226G>A
ENST00000528076.1:c.165+2226G>A
ENST00000532482.1:c.224-287G>A	ENSP00000436101.1:n.224-287G>A
NM_005959.3:c.223+2226G>A	NP_005950.1:n.223+2226G>A
XM_011542839.1:c.223+2226G>A	XP_011541141.1:n.223+2226G>A
XM_011542839.2:c.223+2226G>A	XP_011541141.1:n.223+2226G>A
NM_005959.5:c.223+2226G>A MANE Select	NP_005950.1:n.223+2226G>A