Canonical Allele Identifier: CA983655833
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs71152641
gnomAD v3: 17-40099009-TG-T
gnomAD v4: 17-40099009-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099014del , CM000679.2:g.40099014del GRCh38
NC_000017.10:g.38255267del , CM000679.1:g.38255267del GRCh37
NC_000017.9:g.35508793del NCBI36
NG_033084.1:g.6716del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1054del MANE Select ENSP00000246672.3:n.31+1054del
ENST00000246672.3:c.31+1054del ENSP00000246672.3:n.31+1054del
NM_021724.4:c.31+1054del NP_068370.1:n.31+1054del
NM_021724.5:c.31+1054del MANE Select NP_068370.1:n.31+1054del
Search 100 bp 5'
Search 100 bp 3'