Canonical Allele Identifier: CA2733567449

Gene: NR1D1

Linked Data

• dbSNP Id: rs2145105011

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40098812_40098814del , CM000679.2:g.40098812_40098814del	GRCh38
NC_000017.10:g.38255065_38255067del , CM000679.1:g.38255065_38255067del	GRCh37
NC_000017.9:g.35508591_35508593del	NCBI36
NG_033084.1:g.6912_6914del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+1250_31+1252del MANE Select	ENSP00000246672.3:n.31+1250_31+1252del
ENST00000246672.3:c.31+1250_31+1252del	ENSP00000246672.3:n.31+1250_31+1252del
NM_021724.4:c.31+1250_31+1252del	NP_068370.1:n.31+1250_31+1252del
NM_021724.5:c.31+1250_31+1252del MANE Select	NP_068370.1:n.31+1250_31+1252del