Canonical Allele Identifier: CA771898383
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1229799520
MyVariant Identifiers: chr17:g.38255609C>G (hg19) chr17:g.40099356C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099356C>G , CM000679.2:g.40099356C>G GRCh38
NC_000017.10:g.38255609C>G , CM000679.1:g.38255609C>G GRCh37
NC_000017.9:g.35509135C>G NCBI36
NG_033084.1:g.6370G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+708G>C MANE Select ENSP00000246672.3:n.31+708G>C
ENST00000246672.3:c.31+708G>C ENSP00000246672.3:n.31+708G>C
NM_021724.4:c.31+708G>C NP_068370.1:n.31+708G>C
NM_021724.5:c.31+708G>C MANE Select NP_068370.1:n.31+708G>C
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