Canonical Allele Identifier: CA15680473
Gene: MTNR1B HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.92982683G>A
GRCh37 chr11:g.92715849G>A
gnomAD v2:
11:92715849 G / A
gnomAD v3:
11:92982683 G / A
gnomAD v4:
chr11-92982683-G-A
Joint Max Group AF 0.69131559 (SAS)
Genomes Max Group AF 0.67763673 (SAS)
Exomes Max Group AF 0.69217954 (SAS)
dbSNP:
1562444
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.92982683G>A , CM000673.2:g.92982683G>A GRCh38
NC_000011.9:g.92715849G>A , CM000673.1:g.92715849G>A GRCh37
NC_000011.8:g.92355497G>A NCBI36
NG_028160.1:g.18061G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000257068.3:c.*371G>A MANE Select ENSP00000257068.2:n.*371G>A
ENST00000257068.2:c.*371G>A ENSP00000257068.2:n.*371G>A
ENST00000528076.1:c.166-2124G>A
NM_005959.3:c.*371G>A NP_005950.1:n.*371G>A
XM_011542839.1:c.*371G>A XP_011541141.1:n.*371G>A
XM_011542839.2:c.1460G>A XP_011541141.1:n.1460G>A
XM_017017777.1:c.*371G>A XP_016873266.1:n.*371G>A
NM_005959.5:c.*371G>A MANE Select NP_005950.1:n.*371G>A
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