Canonical Allele Identifier: CA681920798
Gene: MTNR1B HGNC NCBI

Linked Data

dbSNP Id: rs1421887832
MyVariant Identifiers: chr11:g.92705248G>A (hg19) chr11:g.92972082G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.92972082G>A , CM000673.2:g.92972082G>A GRCh38
NC_000011.9:g.92705248G>A , CM000673.1:g.92705248G>A GRCh37
NC_000011.8:g.92344896G>A NCBI36
NG_028160.1:g.7460G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000257068.3:c.223+2134G>A MANE Select ENSP00000257068.2:n.223+2134G>A
ENST00000257068.2:c.223+2134G>A ENSP00000257068.2:n.223+2134G>A
ENST00000528076.1:c.165+2134G>A
ENST00000532482.1:c.224-379G>A ENSP00000436101.1:n.224-379G>A
NM_005959.3:c.223+2134G>A NP_005950.1:n.223+2134G>A
XM_011542839.1:c.223+2134G>A XP_011541141.1:n.223+2134G>A
XM_011542839.2:c.223+2134G>A XP_011541141.1:n.223+2134G>A
NM_005959.5:c.223+2134G>A MANE Select NP_005950.1:n.223+2134G>A
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