Canonical Allele Identifier: CA123266256
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs376455050
gnomAD v2: 5-92921103-A-G
gnomAD v4: 5-93585397-A-G
MyVariant Identifiers: chr5:g.92921103A>G (hg19) chr5:g.93585397A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585397A>G , CM000667.2:g.93585397A>G GRCh38
NC_000005.9:g.92921103A>G , CM000667.1:g.92921103A>G GRCh37
NC_000005.8:g.92946859A>G NCBI36
NG_034119.1:g.7061A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.299A>G ENSP00000481517.1:p.Asn100Ser
ENST00000327111.8:c.374A>G MANE Select ENSP00000325819.3:p.Asn125Ser
ENST00000647447.1:c.221A>G ENSP00000495740.1:p.Asn74Ser
ENST00000327111.7:c.374A>G ENSP00000325819.3:p.Asn125Ser
ENST00000615873.1:c.299A>G ENSP00000481517.1:p.Asn100Ser
NM_005654.5:c.374A>G NP_005645.1:p.Asn125Ser
NM_005654.6:c.374A>G MANE Select NP_005645.1:p.Asn125Ser
Search 100 bp 5'
Search 100 bp 3'