Canonical Allele Identifier: CA360526142
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585399A>T , CM000667.2:g.93585399A>T GRCh38
NC_000005.9:g.92921105A>T , CM000667.1:g.92921105A>T GRCh37
NC_000005.8:g.92946861A>T NCBI36
NG_034119.1:g.7063A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.301A>T ENSP00000481517.1:p.Arg101Trp
ENST00000327111.8:c.376A>T MANE Select ENSP00000325819.3:p.Arg126Trp
ENST00000647447.1:c.223A>T ENSP00000495740.1:p.Arg75Trp
ENST00000327111.7:c.376A>T ENSP00000325819.3:p.Arg126Trp
ENST00000615873.1:c.301A>T ENSP00000481517.1:p.Arg101Trp
NM_005654.5:c.376A>T NP_005645.1:p.Arg126Trp
NM_005654.6:c.376A>T MANE Select NP_005645.1:p.Arg126Trp