Canonical Allele Identifier: CA2259395211

Gene: NR1D1

Linked Data

• dbSNP Id: rs1987823034

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40099104G>T , CM000679.2:g.40099104G>T	GRCh38
NC_000017.10:g.38255357G>T , CM000679.1:g.38255357G>T	GRCh37
NC_000017.9:g.35508883G>T	NCBI36
NG_033084.1:g.6622C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+960C>A MANE Select	ENSP00000246672.3:n.31+960C>A
ENST00000246672.3:c.31+960C>A	ENSP00000246672.3:n.31+960C>A
NM_021724.4:c.31+960C>A	NP_068370.1:n.31+960C>A
NM_021724.5:c.31+960C>A MANE Select	NP_068370.1:n.31+960C>A