Canonical Allele Identifier: CA2259395007
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1987814740
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098817_40098838dup , CM000679.2:g.40098817_40098838dup GRCh38
NC_000017.10:g.38255070_38255091dup , CM000679.1:g.38255070_38255091dup GRCh37
NC_000017.9:g.35508596_35508617dup NCBI36
NG_033084.1:g.6892_6913dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1230_31+1251dup MANE Select ENSP00000246672.3:n.31+1230_31+1251dup
ENST00000246672.3:c.31+1230_31+1251dup ENSP00000246672.3:n.31+1230_31+1251dup
NM_021724.4:c.31+1230_31+1251dup NP_068370.1:n.31+1230_31+1251dup
NM_021724.5:c.31+1230_31+1251dup MANE Select NP_068370.1:n.31+1230_31+1251dup
Search 100 bp 5'
Search 100 bp 3'