Canonical Allele Identifier: CA360526121
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585389C>G , CM000667.2:g.93585389C>G GRCh38
NC_000005.9:g.92921095C>G , CM000667.1:g.92921095C>G GRCh37
NC_000005.8:g.92946851C>G NCBI36
NG_034119.1:g.7053C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.291C>G ENSP00000481517.1:p.Cys97Trp
ENST00000327111.8:c.366C>G MANE Select ENSP00000325819.3:p.Cys122Trp
ENST00000647447.1:c.213C>G ENSP00000495740.1:p.Cys71Trp
ENST00000327111.7:c.366C>G ENSP00000325819.3:p.Cys122Trp
ENST00000615873.1:c.291C>G ENSP00000481517.1:p.Cys97Trp
NM_005654.5:c.366C>G NP_005645.1:p.Cys122Trp
NM_005654.6:c.366C>G MANE Select NP_005645.1:p.Cys122Trp