Canonical Allele Identifier: CA1564182852
Gene: NR2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585400G= , CM000667.2:g.93585400G= GRCh38
NC_000005.9:g.92921106G= , CM000667.1:g.92921106G= GRCh37
NC_000005.8:g.92946862G= NCBI36
NG_034119.1:g.7064G=

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.302G= ENSP00000481517.1:p.Arg101=
ENST00000327111.8:c.377G= MANE Select ENSP00000325819.3:p.Arg126=
ENST00000647447.1:c.224G= ENSP00000495740.1:p.Arg75=
ENST00000327111.7:c.377G= ENSP00000325819.3:p.Arg126=
ENST00000615873.1:c.302G= ENSP00000481517.1:p.Arg101=
NM_005654.5:c.377G= NP_005645.1:p.Arg126=
NM_005654.6:c.377G= MANE Select NP_005645.1:p.Arg126=