Canonical Allele Identifier: CA1564182816
Gene: NR2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585299G= , CM000667.2:g.93585299G= GRCh38
NC_000005.9:g.92921005G= , CM000667.1:g.92921005G= GRCh37
NC_000005.8:g.92946761G= NCBI36
NG_034119.1:g.6963G=

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.201G= ENSP00000481517.1:p.Lys67=
ENST00000327111.8:c.276G= MANE Select ENSP00000325819.3:p.Lys92=
ENST00000647447.1:c.123G= ENSP00000495740.1:p.Lys41=
ENST00000327111.7:c.276G= ENSP00000325819.3:p.Lys92=
ENST00000615873.1:c.201G= ENSP00000481517.1:p.Lys67=
NM_005654.5:c.276G= NP_005645.1:p.Lys92=
NM_005654.6:c.276G= MANE Select NP_005645.1:p.Lys92=