Canonical Allele Identifier: CA771898270
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1200761563
gnomAD v3: 17-40099193-G-GGA
gnomAD v4: 17-40099193-G-GGA
MyVariant Identifiers: chr17:g.38255446_38255447insGA (hg19) chr17:g.40099193_40099194insGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099194_40099195insAG , CM000679.2:g.40099194_40099195insAG GRCh38
NC_000017.10:g.38255447_38255448insAG , CM000679.1:g.38255447_38255448insAG GRCh37
NC_000017.9:g.35508973_35508974insAG NCBI36
NG_033084.1:g.6532_6533insTC

Transcript Alleles

HGVS Amino-acid change
ENST00000246672.4:c.31+870_31+871insTC MANE Select ENSP00000246672.3:n.31+870_31+871insTC
ENST00000246672.3:c.31+870_31+871insTC ENSP00000246672.3:n.31+870_31+871insTC
NM_021724.4:c.31+870_31+871insTC NP_068370.1:n.31+870_31+871insTC
NM_021724.5:c.31+870_31+871insTC MANE Select NP_068370.1:n.31+870_31+871insTC
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