Canonical Allele Identifier: CA771898396
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1454724606
MyVariant Identifiers: chr17:g.38255642C>A (hg19) chr17:g.40099389C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099389C>A , CM000679.2:g.40099389C>A GRCh38
NC_000017.10:g.38255642C>A , CM000679.1:g.38255642C>A GRCh37
NC_000017.9:g.35509168C>A NCBI36
NG_033084.1:g.6337G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+675G>T MANE Select ENSP00000246672.3:n.31+675G>T
ENST00000246672.3:c.31+675G>T ENSP00000246672.3:n.31+675G>T
NM_021724.4:c.31+675G>T NP_068370.1:n.31+675G>T
NM_021724.5:c.31+675G>T MANE Select NP_068370.1:n.31+675G>T
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