Canonical Allele Identifier: CA276169624
Gene: NR2F2 HGNC NCBI
NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs200310787
MyVariant Identifiers: chr15:g.96869607T>C (hg19) chr15:g.96326378T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96326378T>C , CM000677.2:g.96326378T>C GRCh38
NC_000015.9:g.96869607T>C , CM000677.1:g.96869607T>C GRCh37
NC_000015.8:g.94670611T>C NCBI36
NG_016753.1:g.5451T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000421109.6:c.43+26T>C (NR2F2) ENSP00000401674.2:n.43+26T>C
NM_001145155.1:c.43+26T>C (NR2F2) NP_001138627.1:n.43+26T>C
NR_102743.1:n.163+821A>G (NR2F2-AS1)
NR_102744.1:n.163+821A>G (NR2F2-AS1)
NR_125738.1:n.163+578A>G (NR2F2-AS1)
NM_001145155.2:c.43+26T>C (NR2F2) NP_001138627.1:n.43+26T>C
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