Canonical Allele Identifier: CA360525886
Gene: NR2F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.92920996C>G (hg19) chr5:g.93585290C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585290C>G , CM000667.2:g.93585290C>G GRCh38
NC_000005.9:g.92920996C>G , CM000667.1:g.92920996C>G GRCh37
NC_000005.8:g.92946752C>G NCBI36
NG_034119.1:g.6954C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.192C>G ENSP00000481517.1:p.Cys64Trp
ENST00000327111.8:c.267C>G MANE Select ENSP00000325819.3:p.Cys89Trp
ENST00000647447.1:c.114C>G ENSP00000495740.1:p.Cys38Trp
ENST00000327111.7:c.267C>G ENSP00000325819.3:p.Cys89Trp
ENST00000615873.1:c.192C>G ENSP00000481517.1:p.Cys64Trp
NM_005654.5:c.267C>G NP_005645.1:p.Cys89Trp
NM_005654.6:c.267C>G MANE Select NP_005645.1:p.Cys89Trp
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