Canonical Allele Identifier: CA360525883
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585289G>T , CM000667.2:g.93585289G>T GRCh38
NC_000005.9:g.92920995G>T , CM000667.1:g.92920995G>T GRCh37
NC_000005.8:g.92946751G>T NCBI36
NG_034119.1:g.6953G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.191G>T ENSP00000481517.1:p.Cys64Phe
ENST00000327111.8:c.266G>T MANE Select ENSP00000325819.3:p.Cys89Phe
ENST00000647447.1:c.113G>T ENSP00000495740.1:p.Cys38Phe
ENST00000327111.7:c.266G>T ENSP00000325819.3:p.Cys89Phe
ENST00000615873.1:c.191G>T ENSP00000481517.1:p.Cys64Phe
NM_005654.5:c.266G>T NP_005645.1:p.Cys89Phe
NM_005654.6:c.266G>T MANE Select NP_005645.1:p.Cys89Phe