Canonical Allele Identifier: CA360526013
Gene: NR2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585343A>G , CM000667.2:g.93585343A>G GRCh38
NC_000005.9:g.92921049A>G , CM000667.1:g.92921049A>G GRCh37
NC_000005.8:g.92946805A>G NCBI36
NG_034119.1:g.7007A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005654.6:c.320A>G MANE Select NP_005645.1:p.Lys107Arg
ENST00000327111.8:c.320A>G MANE Select ENSP00000325819.3:p.Lys107Arg
NM_005654.5:c.320A>G NP_005645.1:p.Lys107Arg
ENST00000327111.7:c.320A>G ENSP00000325819.3:p.Lys107Arg
ENST00000615873.1:c.245A>G ENSP00000481517.1:p.Lys82Arg
ENST00000615873.2:c.245A>G ENSP00000481517.1:p.Lys82Arg
ENST00000647447.1:c.167A>G ENSP00000495740.1:p.Lys56Arg