Canonical Allele Identifier: CA2259395145
Gene: NR1D1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099035C= , CM000679.2:g.40099035C= GRCh38
NC_000017.10:g.38255288C= , CM000679.1:g.38255288C= GRCh37
NC_000017.9:g.35508814C= NCBI36
NG_033084.1:g.6691G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1029G= MANE Select ENSP00000246672.3:n.31+1029G=
ENST00000246672.3:c.31+1029G= ENSP00000246672.3:n.31+1029G=
NM_021724.4:c.31+1029G= NP_068370.1:n.31+1029G=
NM_021724.5:c.31+1029G= MANE Select NP_068370.1:n.31+1029G=
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