Canonical Allele Identifier: CA360525885
Gene: NR2F1 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.192C>A ENSP00000481517.1:p.Cys64Ter
ENST00000327111.8:c.267C>A MANE Select ENSP00000325819.3:p.Cys89Ter
ENST00000647447.1:c.114C>A ENSP00000495740.1:p.Cys38Ter
ENST00000327111.7:c.267C>A ENSP00000325819.3:p.Cys89Ter
ENST00000615873.1:c.192C>A ENSP00000481517.1:p.Cys64Ter
NM_005654.5:c.267C>A NP_005645.1:p.Cys89Ter
NM_005654.6:c.267C>A MANE Select NP_005645.1:p.Cys89Ter
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