Canonical Allele Identifier: CA445569990
Gene: NR2F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.92921098T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585392T>G , CM000667.2:g.93585392T>G GRCh38
NC_000005.9:g.92921098T>G , CM000667.1:g.92921098T>G GRCh37
NC_000005.8:g.92946854T>G NCBI36
NG_034119.1:g.7056T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.294T>G ENSP00000481517.1:p.Arg98=
ENST00000327111.8:c.369T>G MANE Select ENSP00000325819.3:p.Arg123=
ENST00000647447.1:c.216T>G ENSP00000495740.1:p.Arg72=
ENST00000327111.7:c.369T>G ENSP00000325819.3:p.Arg123=
ENST00000615873.1:c.294T>G ENSP00000481517.1:p.Arg98=
NM_005654.5:c.369T>G NP_005645.1:p.Arg123=
NM_005654.6:c.369T>G MANE Select NP_005645.1:p.Arg123=
Search 100 bp 5'
Search 100 bp 3'