Canonical Allele Identifier: CA360526140
Gene: NR2F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.92921104C>G (hg19) chr5:g.93585398C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585398C>G , CM000667.2:g.93585398C>G GRCh38
NC_000005.9:g.92921104C>G , CM000667.1:g.92921104C>G GRCh37
NC_000005.8:g.92946860C>G NCBI36
NG_034119.1:g.7062C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.300C>G ENSP00000481517.1:p.Asn100Lys
ENST00000327111.8:c.375C>G MANE Select ENSP00000325819.3:p.Asn125Lys
ENST00000647447.1:c.222C>G ENSP00000495740.1:p.Asn74Lys
ENST00000327111.7:c.375C>G ENSP00000325819.3:p.Asn125Lys
ENST00000615873.1:c.300C>G ENSP00000481517.1:p.Asn100Lys
NM_005654.5:c.375C>G NP_005645.1:p.Asn125Lys
NM_005654.6:c.375C>G MANE Select NP_005645.1:p.Asn125Lys
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