Canonical Allele Identifier: CA492689229
Gene: NR2F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.96875592G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96332363G>C , CM000677.2:g.96332363G>C GRCh38
NC_000015.9:g.96875592G>C , CM000677.1:g.96875592G>C GRCh37
NC_000015.8:g.94676596G>C NCBI36
NG_016753.1:g.11436G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000394166.8:c.258G>C MANE Select ENSP00000377721.3:p.Ser86=
ENST00000394166.7:c.258G>C ENSP00000377721.3:p.Ser86=
ENST00000421109.6:c.44-1713G>C ENSP00000401674.2:n.44-1713G>C
NM_001145155.1:c.44-1713G>C NP_001138627.1:n.44-1713G>C
NM_021005.3:c.258G>C NP_066285.1:p.Ser86=
NM_021005.4:c.258G>C MANE Select NP_066285.1:p.Ser86=
NM_001145155.2:c.44-1713G>C NP_001138627.1:n.44-1713G>C
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