Canonical Allele Identifier: CA625964104
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1434016166
gnomAD v2: 17-38255637-G-C
MyVariant Identifiers: chr17:g.38255637G>C (hg19) chr17:g.40099384G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099384G>C , CM000679.2:g.40099384G>C GRCh38
NC_000017.10:g.38255637G>C , CM000679.1:g.38255637G>C GRCh37
NC_000017.9:g.35509163G>C NCBI36
NG_033084.1:g.6342C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000246672.4:c.31+680C>G MANE Select ENSP00000246672.3:n.31+680C>G
ENST00000246672.3:c.31+680C>G ENSP00000246672.3:n.31+680C>G
NM_021724.4:c.31+680C>G NP_068370.1:n.31+680C>G
NM_021724.5:c.31+680C>G MANE Select NP_068370.1:n.31+680C>G
Search 100 bp 5'
Search 100 bp 3'