Canonical Allele Identifier: CA2259395138
Gene: NR1D1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099030C= , CM000679.2:g.40099030C= GRCh38
NC_000017.10:g.38255283C= , CM000679.1:g.38255283C= GRCh37
NC_000017.9:g.35508809C= NCBI36
NG_033084.1:g.6696G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1034G= MANE Select ENSP00000246672.3:n.31+1034G=
ENST00000246672.3:c.31+1034G= ENSP00000246672.3:n.31+1034G=
NM_021724.4:c.31+1034G= NP_068370.1:n.31+1034G=
NM_021724.5:c.31+1034G= MANE Select NP_068370.1:n.31+1034G=
Search 100 bp 5'
Search 100 bp 3'