Canonical Allele Identifier: CA360526115
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585387T>A , CM000667.2:g.93585387T>A GRCh38
NC_000005.9:g.92921093T>A , CM000667.1:g.92921093T>A GRCh37
NC_000005.8:g.92946849T>A NCBI36
NG_034119.1:g.7051T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.289T>A ENSP00000481517.1:p.Cys97Ser
ENST00000327111.8:c.364T>A MANE Select ENSP00000325819.3:p.Cys122Ser
ENST00000647447.1:c.211T>A ENSP00000495740.1:p.Cys71Ser
ENST00000327111.7:c.364T>A ENSP00000325819.3:p.Cys122Ser
ENST00000615873.1:c.289T>A ENSP00000481517.1:p.Cys97Ser
NM_005654.5:c.364T>A NP_005645.1:p.Cys122Ser
NM_005654.6:c.364T>A MANE Select NP_005645.1:p.Cys122Ser