Canonical Allele Identifier: CA360526131
Gene: NR2F1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.296C>A ENSP00000481517.1:p.Ala99Asp
ENST00000327111.8:c.371C>A MANE Select ENSP00000325819.3:p.Ala124Asp
ENST00000647447.1:c.218C>A ENSP00000495740.1:p.Ala73Asp
ENST00000327111.7:c.371C>A ENSP00000325819.3:p.Ala124Asp
ENST00000615873.1:c.296C>A ENSP00000481517.1:p.Ala99Asp
NM_005654.5:c.371C>A NP_005645.1:p.Ala124Asp
NM_005654.6:c.371C>A MANE Select NP_005645.1:p.Ala124Asp