Canonical Allele Identifier: CA2198009591
Gene: NR2F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96332366C= , CM000677.2:g.96332366C= GRCh38
NC_000015.9:g.96875595C= , CM000677.1:g.96875595C= GRCh37
NC_000015.8:g.94676599C= NCBI36
NG_016753.1:g.11439C=

Transcript Alleles

HGVS Amino-acid change
ENST00000394166.8:c.261C= MANE Select ENSP00000377721.3:p.Ser87=
ENST00000394166.7:c.261C= ENSP00000377721.3:p.Ser87=
ENST00000421109.6:c.44-1710C= ENSP00000401674.2:n.44-1710C=
NM_001145155.1:c.44-1710C= NP_001138627.1:n.44-1710C=
NM_021005.3:c.261C= NP_066285.1:p.Ser87=
NM_021005.4:c.261C= MANE Select NP_066285.1:p.Ser87=
NM_001145155.2:c.44-1710C= NP_001138627.1:n.44-1710C=
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