Canonical Allele Identifier: CA2259395121

Gene: NR1D1

Linked Data

• dbSNP Id: rs71152641

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40099013_40099014dup , CM000679.2:g.40099013_40099014dup	GRCh38
NC_000017.10:g.38255266_38255267dup , CM000679.1:g.38255266_38255267dup	GRCh37
NC_000017.9:g.35508792_35508793dup	NCBI36
NG_033084.1:g.6715_6716dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+1053_31+1054dup MANE Select	ENSP00000246672.3:n.31+1053_31+1054dup
ENST00000246672.3:c.31+1053_31+1054dup	ENSP00000246672.3:n.31+1053_31+1054dup
NM_021724.4:c.31+1053_31+1054dup	NP_068370.1:n.31+1053_31+1054dup
NM_021724.5:c.31+1053_31+1054dup MANE Select	NP_068370.1:n.31+1053_31+1054dup