Canonical Allele Identifier: CA2733567479
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs2145105027
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098815G>T , CM000679.2:g.40098815G>T GRCh38
NC_000017.10:g.38255068G>T , CM000679.1:g.38255068G>T GRCh37
NC_000017.9:g.35508594G>T NCBI36
NG_033084.1:g.6911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1249C>A MANE Select ENSP00000246672.3:n.31+1249C>A
ENST00000246672.3:c.31+1249C>A ENSP00000246672.3:n.31+1249C>A
NM_021724.4:c.31+1249C>A NP_068370.1:n.31+1249C>A
NM_021724.5:c.31+1249C>A MANE Select NP_068370.1:n.31+1249C>A
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