Canonical Allele Identifier: CA1564182849
Gene: NR2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585394C= , CM000667.2:g.93585394C= GRCh38
NC_000005.9:g.92921100C= , CM000667.1:g.92921100C= GRCh37
NC_000005.8:g.92946856C= NCBI36
NG_034119.1:g.7058C=

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.296C= ENSP00000481517.1:p.Ala99=
ENST00000327111.8:c.371C= MANE Select ENSP00000325819.3:p.Ala124=
ENST00000647447.1:c.218C= ENSP00000495740.1:p.Ala73=
ENST00000327111.7:c.371C= ENSP00000325819.3:p.Ala124=
ENST00000615873.1:c.296C= ENSP00000481517.1:p.Ala99=
NM_005654.5:c.371C= NP_005645.1:p.Ala124=
NM_005654.6:c.371C= MANE Select NP_005645.1:p.Ala124=