Canonical Allele Identifier: CA360526138
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585397A>T , CM000667.2:g.93585397A>T GRCh38
NC_000005.9:g.92921103A>T , CM000667.1:g.92921103A>T GRCh37
NC_000005.8:g.92946859A>T NCBI36
NG_034119.1:g.7061A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.299A>T ENSP00000481517.1:p.Asn100Ile
ENST00000327111.8:c.374A>T MANE Select ENSP00000325819.3:p.Asn125Ile
ENST00000647447.1:c.221A>T ENSP00000495740.1:p.Asn74Ile
ENST00000327111.7:c.374A>T ENSP00000325819.3:p.Asn125Ile
ENST00000615873.1:c.299A>T ENSP00000481517.1:p.Asn100Ile
NM_005654.5:c.374A>T NP_005645.1:p.Asn125Ile
NM_005654.6:c.374A>T MANE Select NP_005645.1:p.Asn125Ile