Canonical Allele Identifier: CA1564182847
Gene: NR2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585388G= , CM000667.2:g.93585388G= GRCh38
NC_000005.9:g.92921094G= , CM000667.1:g.92921094G= GRCh37
NC_000005.8:g.92946850G= NCBI36
NG_034119.1:g.7052G=

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.290G= ENSP00000481517.1:p.Cys97=
ENST00000327111.8:c.365G= MANE Select ENSP00000325819.3:p.Cys122=
ENST00000647447.1:c.212G= ENSP00000495740.1:p.Cys71=
ENST00000327111.7:c.365G= ENSP00000325819.3:p.Cys122=
ENST00000615873.1:c.290G= ENSP00000481517.1:p.Cys97=
NM_005654.5:c.365G= NP_005645.1:p.Cys122=
NM_005654.6:c.365G= MANE Select NP_005645.1:p.Cys122=