Canonical Allele Identifier: CA360525912
Gene: NR2F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.92921007C>G (hg19) chr5:g.93585301C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585301C>G , CM000667.2:g.93585301C>G GRCh38
NC_000005.9:g.92921007C>G , CM000667.1:g.92921007C>G GRCh37
NC_000005.8:g.92946763C>G NCBI36
NG_034119.1:g.6965C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.203C>G ENSP00000481517.1:p.Ser68Trp
ENST00000327111.8:c.278C>G MANE Select ENSP00000325819.3:p.Ser93Trp
ENST00000647447.1:c.125C>G ENSP00000495740.1:p.Ser42Trp
ENST00000327111.7:c.278C>G ENSP00000325819.3:p.Ser93Trp
ENST00000615873.1:c.203C>G ENSP00000481517.1:p.Ser68Trp
NM_005654.5:c.278C>G NP_005645.1:p.Ser93Trp
NM_005654.6:c.278C>G MANE Select NP_005645.1:p.Ser93Trp
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