Canonical Allele Identifier: CA1564182812
Gene: NR2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585288T= , CM000667.2:g.93585288T= GRCh38
NC_000005.9:g.92920994T= , CM000667.1:g.92920994T= GRCh37
NC_000005.8:g.92946750T= NCBI36
NG_034119.1:g.6952T=

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.190T= ENSP00000481517.1:p.Cys64=
ENST00000327111.8:c.265T= MANE Select ENSP00000325819.3:p.Cys89=
ENST00000647447.1:c.112T= ENSP00000495740.1:p.Cys38=
ENST00000327111.7:c.265T= ENSP00000325819.3:p.Cys89=
ENST00000615873.1:c.190T= ENSP00000481517.1:p.Cys64=
NM_005654.5:c.265T= NP_005645.1:p.Cys89=
NM_005654.6:c.265T= MANE Select NP_005645.1:p.Cys89=