Canonical Allele Identifier: CA983655828
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs2034111227
gnomAD v3: 17-40099008-A-AG
gnomAD v4: 17-40099008-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099008_40099009insG , CM000679.2:g.40099008_40099009insG GRCh38
NC_000017.10:g.38255261_38255262insG , CM000679.1:g.38255261_38255262insG GRCh37
NC_000017.9:g.35508787_35508788insG NCBI36
NG_033084.1:g.6717_6718insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1055_31+1056insC MANE Select ENSP00000246672.3:n.31+1055_31+1056insC
ENST00000246672.3:c.31+1055_31+1056insC ENSP00000246672.3:n.31+1055_31+1056insC
NM_021724.4:c.31+1055_31+1056insC NP_068370.1:n.31+1055_31+1056insC
NM_021724.5:c.31+1055_31+1056insC MANE Select NP_068370.1:n.31+1055_31+1056insC
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