Canonical Allele Identifier: CA393929380

Gene: NR2F2 NR2F2-AS1

Linked Data

• ClinVar Variation Id: 426710
• ClinVar RCV Id: RCV000490137
• dbSNP Id: rs1085307757
• gnomAD v2: 15-96869582-G-A
• gnomAD v3: 15-96326353-G-A
• gnomAD v4: 15-96326353-G-A
• MyVariant Identifiers: chr15:g.96869582G>A (hg19) ; chr15:g.96326353G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96326353G>A , CM000677.2:g.96326353G>A	GRCh38
NC_000015.9:g.96869582G>A , CM000677.1:g.96869582G>A	GRCh37
NC_000015.8:g.94670586G>A	NCBI36
NG_016753.1:g.5426G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000421109.6:c.43+1G>A (NR2F2)	ENSP00000401674.2:n.43+1G>A
NM_001145155.1:c.43+1G>A (NR2F2)	NP_001138627.1:n.43+1G>A
NR_102743.1:n.163+846C>T (NR2F2-AS1)
NR_102744.1:n.163+846C>T (NR2F2-AS1)
NR_125738.1:n.163+603C>T (NR2F2-AS1)
NM_001145155.2:c.43+1G>A (NR2F2)	NP_001138627.1:n.43+1G>A