Canonical Allele Identifier: CA290497526
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs767595627
gnomAD v2: 17-38255601-C-CG
gnomAD v3: 17-40099348-C-CG
gnomAD v4: 17-40099348-C-CG
MyVariant Identifiers: chr17:g.38255601_38255602insG (hg19) chr17:g.40099348_40099349insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099355dup , CM000679.2:g.40099355dup GRCh38
NC_000017.10:g.38255608dup , CM000679.1:g.38255608dup GRCh37
NC_000017.9:g.35509134dup NCBI36
NG_033084.1:g.6377dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+715dup MANE Select ENSP00000246672.3:n.31+715dup
ENST00000246672.3:c.31+715dup ENSP00000246672.3:n.31+715dup
NM_021724.4:c.31+715dup NP_068370.1:n.31+715dup
NM_021724.5:c.31+715dup MANE Select NP_068370.1:n.31+715dup
Search 100 bp 5'
Search 100 bp 3'