Canonical Allele Identifier: CA2259395063
Gene: NR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098915G= , CM000679.2:g.40098915G= GRCh38
NC_000017.10:g.38255168G= , CM000679.1:g.38255168G= GRCh37
NC_000017.9:g.35508694G= NCBI36
NG_033084.1:g.6811C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1149C= MANE Select ENSP00000246672.3:n.31+1149C=
ENST00000246672.3:c.31+1149C= ENSP00000246672.3:n.31+1149C=
NM_021724.4:c.31+1149C= NP_068370.1:n.31+1149C=
NM_021724.5:c.31+1149C= MANE Select NP_068370.1:n.31+1149C=