Canonical Allele Identifier: CA2259395030
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1987815690

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098849dup , CM000679.2:g.40098849dup GRCh38
NC_000017.10:g.38255102dup , CM000679.1:g.38255102dup GRCh37
NC_000017.9:g.35508628dup NCBI36
NG_033084.1:g.6877dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1215dup MANE Select ENSP00000246672.3:n.31+1215dup
ENST00000246672.3:c.31+1215dup ENSP00000246672.3:n.31+1215dup
NM_021724.4:c.31+1215dup NP_068370.1:n.31+1215dup
NM_021724.5:c.31+1215dup MANE Select NP_068370.1:n.31+1215dup