Canonical Allele Identifier: CA2259394998
Gene: NR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098805C= , CM000679.2:g.40098805C= GRCh38
NC_000017.10:g.38255058C= , CM000679.1:g.38255058C= GRCh37
NC_000017.9:g.35508584C= NCBI36
NG_033084.1:g.6921G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1259G= MANE Select ENSP00000246672.3:n.31+1259G=
ENST00000246672.3:c.31+1259G= ENSP00000246672.3:n.31+1259G=
NM_021724.4:c.31+1259G= NP_068370.1:n.31+1259G=
NM_021724.5:c.31+1259G= MANE Select NP_068370.1:n.31+1259G=