Canonical Allele Identifier: CA2259395126
Gene: NR1D1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099013G= , CM000679.2:g.40099013G= GRCh38
NC_000017.10:g.38255266G= , CM000679.1:g.38255266G= GRCh37
NC_000017.9:g.35508792G= NCBI36
NG_033084.1:g.6713C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1051C= MANE Select ENSP00000246672.3:n.31+1051C=
ENST00000246672.3:c.31+1051C= ENSP00000246672.3:n.31+1051C=
NM_021724.4:c.31+1051C= NP_068370.1:n.31+1051C=
NM_021724.5:c.31+1051C= MANE Select NP_068370.1:n.31+1051C=
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