Canonical Allele Identifier: CA1564182850
Gene: NR2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585395C= , CM000667.2:g.93585395C= GRCh38
NC_000005.9:g.92921101C= , CM000667.1:g.92921101C= GRCh37
NC_000005.8:g.92946857C= NCBI36
NG_034119.1:g.7059C=

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.297C= ENSP00000481517.1:p.Ala99=
ENST00000327111.8:c.372C= MANE Select ENSP00000325819.3:p.Ala124=
ENST00000647447.1:c.219C= ENSP00000495740.1:p.Ala73=
ENST00000327111.7:c.372C= ENSP00000325819.3:p.Ala124=
ENST00000615873.1:c.297C= ENSP00000481517.1:p.Ala99=
NM_005654.5:c.372C= NP_005645.1:p.Ala124=
NM_005654.6:c.372C= MANE Select NP_005645.1:p.Ala124=