Canonical Allele Identifier: CA360526118
Gene: NR2F1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2229340
ClinVar RCV Id: RCV002692671 RCV003228126
MyVariant Identifiers: chr5:g.92921094G>A (hg19) chr5:g.93585388G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585388G>A , CM000667.2:g.93585388G>A GRCh38
NC_000005.9:g.92921094G>A , CM000667.1:g.92921094G>A GRCh37
NC_000005.8:g.92946850G>A NCBI36
NG_034119.1:g.7052G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.290G>A ENSP00000481517.1:p.Cys97Tyr
ENST00000327111.8:c.365G>A MANE Select ENSP00000325819.3:p.Cys122Tyr
ENST00000647447.1:c.212G>A ENSP00000495740.1:p.Cys71Tyr
ENST00000327111.7:c.365G>A ENSP00000325819.3:p.Cys122Tyr
ENST00000615873.1:c.290G>A ENSP00000481517.1:p.Cys97Tyr
NM_005654.5:c.365G>A NP_005645.1:p.Cys122Tyr
NM_005654.6:c.365G>A MANE Select NP_005645.1:p.Cys122Tyr
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