Canonical Allele Identifier: CA771897923
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1275157724
MyVariant Identifiers: chr17:g.38255080_38255081insG (hg19) chr17:g.40098827_40098828insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098831dup , CM000679.2:g.40098831dup GRCh38
NC_000017.10:g.38255084dup , CM000679.1:g.38255084dup GRCh37
NC_000017.9:g.35508610dup NCBI36
NG_033084.1:g.6898dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1236dup MANE Select ENSP00000246672.3:n.31+1236dup
ENST00000246672.3:c.31+1236dup ENSP00000246672.3:n.31+1236dup
NM_021724.4:c.31+1236dup NP_068370.1:n.31+1236dup
NM_021724.5:c.31+1236dup MANE Select NP_068370.1:n.31+1236dup
Search 100 bp 5'
Search 100 bp 3'