Canonical Allele Identifier: CA360526134
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585396A>C , CM000667.2:g.93585396A>C GRCh38
NC_000005.9:g.92921102A>C , CM000667.1:g.92921102A>C GRCh37
NC_000005.8:g.92946858A>C NCBI36
NG_034119.1:g.7060A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.298A>C ENSP00000481517.1:p.Asn100His
ENST00000327111.8:c.373A>C MANE Select ENSP00000325819.3:p.Asn125His
ENST00000647447.1:c.220A>C ENSP00000495740.1:p.Asn74His
ENST00000327111.7:c.373A>C ENSP00000325819.3:p.Asn125His
ENST00000615873.1:c.298A>C ENSP00000481517.1:p.Asn100His
NM_005654.5:c.373A>C NP_005645.1:p.Asn125His
NM_005654.6:c.373A>C MANE Select NP_005645.1:p.Asn125His