Canonical Allele Identifier: CA771898320
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1472524098
MyVariant Identifiers: chr17:g.38255516C>T (hg19) chr17:g.40099263C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099263C>T , CM000679.2:g.40099263C>T GRCh38
NC_000017.10:g.38255516C>T , CM000679.1:g.38255516C>T GRCh37
NC_000017.9:g.35509042C>T NCBI36
NG_033084.1:g.6463G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000246672.4:c.31+801G>A MANE Select ENSP00000246672.3:n.31+801G>A
ENST00000246672.3:c.31+801G>A ENSP00000246672.3:n.31+801G>A
NM_021724.4:c.31+801G>A NP_068370.1:n.31+801G>A
NM_021724.5:c.31+801G>A MANE Select NP_068370.1:n.31+801G>A
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