Canonical Allele Identifier: CA360526135
Gene: NR2F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.92921102A>G (hg19) chr5:g.93585396A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585396A>G , CM000667.2:g.93585396A>G GRCh38
NC_000005.9:g.92921102A>G , CM000667.1:g.92921102A>G GRCh37
NC_000005.8:g.92946858A>G NCBI36
NG_034119.1:g.7060A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.298A>G ENSP00000481517.1:p.Asn100Asp
ENST00000327111.8:c.373A>G MANE Select ENSP00000325819.3:p.Asn125Asp
ENST00000647447.1:c.220A>G ENSP00000495740.1:p.Asn74Asp
ENST00000327111.7:c.373A>G ENSP00000325819.3:p.Asn125Asp
ENST00000615873.1:c.298A>G ENSP00000481517.1:p.Asn100Asp
NM_005654.5:c.373A>G NP_005645.1:p.Asn125Asp
NM_005654.6:c.373A>G MANE Select NP_005645.1:p.Asn125Asp
Search 100 bp 5'
Search 100 bp 3'