Canonical Allele Identifier: CA1564182851
Gene: NR2F1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.299A= ENSP00000481517.1:p.Asn100=
ENST00000327111.8:c.374A= MANE Select ENSP00000325819.3:p.Asn125=
ENST00000647447.1:c.221A= ENSP00000495740.1:p.Asn74=
ENST00000327111.7:c.374A= ENSP00000325819.3:p.Asn125=
ENST00000615873.1:c.299A= ENSP00000481517.1:p.Asn100=
NM_005654.5:c.374A= NP_005645.1:p.Asn125=
NM_005654.6:c.374A= MANE Select NP_005645.1:p.Asn125=