Canonical Allele Identifier: CA226956138
Gene: MTNR1B HGNC NCBI

Linked Data

dbSNP Id: rs967776991
gnomAD v2: 11-92705136-C-T
gnomAD v3: 11-92971970-C-T
gnomAD v4: 11-92971970-C-T
MyVariant Identifiers: chr11:g.92705136C>T (hg19) chr11:g.92971970C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.92971970C>T , CM000673.2:g.92971970C>T GRCh38
NC_000011.9:g.92705136C>T , CM000673.1:g.92705136C>T GRCh37
NC_000011.8:g.92344784C>T NCBI36
NG_028160.1:g.7348C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000257068.3:c.223+2022C>T MANE Select ENSP00000257068.2:n.223+2022C>T
ENST00000257068.2:c.223+2022C>T ENSP00000257068.2:n.223+2022C>T
ENST00000528076.1:c.165+2022C>T
ENST00000532482.1:c.224-491C>T ENSP00000436101.1:n.224-491C>T
NM_005959.3:c.223+2022C>T NP_005950.1:n.223+2022C>T
XM_011542839.1:c.223+2022C>T XP_011541141.1:n.223+2022C>T
XM_011542839.2:c.223+2022C>T XP_011541141.1:n.223+2022C>T
NM_005959.5:c.223+2022C>T MANE Select NP_005950.1:n.223+2022C>T
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