Canonical Allele Identifier: CA360525888
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585291G>C , CM000667.2:g.93585291G>C GRCh38
NC_000005.9:g.92920997G>C , CM000667.1:g.92920997G>C GRCh37
NC_000005.8:g.92946753G>C NCBI36
NG_034119.1:g.6955G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.193G>C ENSP00000481517.1:p.Gly65Arg
ENST00000327111.8:c.268G>C MANE Select ENSP00000325819.3:p.Gly90Arg
ENST00000647447.1:c.115G>C ENSP00000495740.1:p.Gly39Arg
ENST00000327111.7:c.268G>C ENSP00000325819.3:p.Gly90Arg
ENST00000615873.1:c.193G>C ENSP00000481517.1:p.Gly65Arg
NM_005654.5:c.268G>C NP_005645.1:p.Gly90Arg
NM_005654.6:c.268G>C MANE Select NP_005645.1:p.Gly90Arg