Canonical Allele Identifier: CA360525884
Gene: NR2F1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2441915
ClinVar RCV Id: RCV003148230
gnomAD v4: 5-93585289-G-A
MyVariant Identifiers: chr5:g.92920995G>A (hg19) chr5:g.93585289G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585289G>A , CM000667.2:g.93585289G>A GRCh38
NC_000005.9:g.92920995G>A , CM000667.1:g.92920995G>A GRCh37
NC_000005.8:g.92946751G>A NCBI36
NG_034119.1:g.6953G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.191G>A ENSP00000481517.1:p.Cys64Tyr
ENST00000327111.8:c.266G>A MANE Select ENSP00000325819.3:p.Cys89Tyr
ENST00000647447.1:c.113G>A ENSP00000495740.1:p.Cys38Tyr
ENST00000327111.7:c.266G>A ENSP00000325819.3:p.Cys89Tyr
ENST00000615873.1:c.191G>A ENSP00000481517.1:p.Cys64Tyr
NM_005654.5:c.266G>A NP_005645.1:p.Cys89Tyr
NM_005654.6:c.266G>A MANE Select NP_005645.1:p.Cys89Tyr
Search 100 bp 5'
Search 100 bp 3'