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ClinGen Allele Registry
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Canonical Allele Identifier:
CA2259395381
Community Standard Title: NM_021724.5(NR1D1):c.31+723C=
Gene: NR1D1
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.40099341G= , CM000679.2:g.40099341G=
GRCh38
NC_000017.10:g.38255594G= , CM000679.1:g.38255594G=
GRCh37
NC_000017.9:g.35509120G=
NCBI36
NG_033084.1:g.6385C=
Transcript Alleles
HGVS
Amino-acid Change
NM_021724.5:c.31+723C=
MANE Select
NP_068370.1:n.31+723C=
ENST00000246672.4:c.31+723C=
MANE Select
ENSP00000246672.3:n.31+723C=
NM_021724.4:c.31+723C=
NP_068370.1:n.31+723C=
ENST00000246672.3:c.31+723C=
ENSP00000246672.3:n.31+723C=
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