Canonical Allele Identifier: CA2259395117
Gene: NR1D1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099008A= , CM000679.2:g.40099008A= GRCh38
NC_000017.10:g.38255261A= , CM000679.1:g.38255261A= GRCh37
NC_000017.9:g.35508787A= NCBI36
NG_033084.1:g.6718T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1056T= MANE Select ENSP00000246672.3:n.31+1056T=
ENST00000246672.3:c.31+1056T= ENSP00000246672.3:n.31+1056T=
NM_021724.4:c.31+1056T= NP_068370.1:n.31+1056T=
NM_021724.5:c.31+1056T= MANE Select NP_068370.1:n.31+1056T=
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