Canonical Allele Identifier: CA393929949
Gene: NR2F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.96875593A>C (hg19) chr15:g.96332364A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96332364A>C , CM000677.2:g.96332364A>C GRCh38
NC_000015.9:g.96875593A>C , CM000677.1:g.96875593A>C GRCh37
NC_000015.8:g.94676597A>C NCBI36
NG_016753.1:g.11437A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000394166.8:c.259A>C MANE Select ENSP00000377721.3:p.Ser87Arg
ENST00000394166.7:c.259A>C ENSP00000377721.3:p.Ser87Arg
ENST00000421109.6:c.44-1712A>C ENSP00000401674.2:n.44-1712A>C
NM_001145155.1:c.44-1712A>C NP_001138627.1:n.44-1712A>C
NM_021005.3:c.259A>C NP_066285.1:p.Ser87Arg
NM_021005.4:c.259A>C MANE Select NP_066285.1:p.Ser87Arg
NM_001145155.2:c.44-1712A>C NP_001138627.1:n.44-1712A>C
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