Canonical Allele Identifier: CA2198009589
Gene: NR2F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96332358A= , CM000677.2:g.96332358A= GRCh38
NC_000015.9:g.96875587A= , CM000677.1:g.96875587A= GRCh37
NC_000015.8:g.94676591A= NCBI36
NG_016753.1:g.11431A=

Transcript Alleles

HGVS Amino-acid change
ENST00000394166.8:c.253A= MANE Select ENSP00000377721.3:p.Lys85=
ENST00000394166.7:c.253A= ENSP00000377721.3:p.Lys85=
ENST00000421109.6:c.44-1718A= ENSP00000401674.2:n.44-1718A=
NM_001145155.1:c.44-1718A= NP_001138627.1:n.44-1718A=
NM_021005.3:c.253A= NP_066285.1:p.Lys85=
NM_021005.4:c.253A= MANE Select NP_066285.1:p.Lys85=
NM_001145155.2:c.44-1718A= NP_001138627.1:n.44-1718A=
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