Canonical Allele Identifier: CA360526123
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs1258374008
gnomAD v2: 5-92921096-C-G
gnomAD v4: 5-93585390-C-G
MyVariant Identifiers: chr5:g.92921096C>G (hg19) chr5:g.93585390C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585390C>G , CM000667.2:g.93585390C>G GRCh38
NC_000005.9:g.92921096C>G , CM000667.1:g.92921096C>G GRCh37
NC_000005.8:g.92946852C>G NCBI36
NG_034119.1:g.7054C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.292C>G ENSP00000481517.1:p.Arg98Gly
ENST00000327111.8:c.367C>G MANE Select ENSP00000325819.3:p.Arg123Gly
ENST00000647447.1:c.214C>G ENSP00000495740.1:p.Arg72Gly
ENST00000327111.7:c.367C>G ENSP00000325819.3:p.Arg123Gly
ENST00000615873.1:c.292C>G ENSP00000481517.1:p.Arg98Gly
NM_005654.5:c.367C>G NP_005645.1:p.Arg123Gly
NM_005654.6:c.367C>G MANE Select NP_005645.1:p.Arg123Gly
Search 100 bp 5'
Search 100 bp 3'