Canonical Allele Identifier: CA445569997
Gene: NR2F1 HGNC NCBI

Linked Data

COSMIC: COSM27195
MyVariant Identifiers: chr5:g.92921107G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585401G>A , CM000667.2:g.93585401G>A GRCh38
NC_000005.9:g.92921107G>A , CM000667.1:g.92921107G>A GRCh37
NC_000005.8:g.92946863G>A NCBI36
NG_034119.1:g.7065G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.303G>A ENSP00000481517.1:p.Arg101=
ENST00000327111.8:c.378G>A MANE Select ENSP00000325819.3:p.Arg126=
ENST00000647447.1:c.225G>A ENSP00000495740.1:p.Arg75=
ENST00000327111.7:c.378G>A ENSP00000325819.3:p.Arg126=
ENST00000615873.1:c.303G>A ENSP00000481517.1:p.Arg101=
NM_005654.5:c.378G>A NP_005645.1:p.Arg126=
NM_005654.6:c.378G>A MANE Select NP_005645.1:p.Arg126=
Search 100 bp 5'
Search 100 bp 3'