Canonical Allele Identifier: CA7750643
Gene: NR2F2 HGNC NCBI
NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs749877354
ExAC: 15:96869604 TTCTC / T
gnomAD v2: 15-96869604-TTCTC-T
gnomAD v3: 15-96326375-TTCTC-T
gnomAD v4: 15-96326375-TTCTC-T
MyVariant Identifiers: chr15:g.96869605_96869608del (hg19) chr15:g.96326376_96326379del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96326383_96326386del , CM000677.2:g.96326383_96326386del GRCh38
NC_000015.9:g.96869612_96869615del , CM000677.1:g.96869612_96869615del GRCh37
NC_000015.8:g.94670616_94670619del NCBI36
NG_016753.1:g.5456_5459del

Transcript Alleles

HGVS Amino-acid Change
ENST00000421109.6:c.43+31_43+34del (NR2F2) ENSP00000401674.2:n.43+31_43+34del
NM_001145155.1:c.43+31_43+34del (NR2F2) NP_001138627.1:n.43+31_43+34del
NR_102743.1:n.163+820_163+823del (NR2F2-AS1)
NR_102744.1:n.163+820_163+823del (NR2F2-AS1)
NR_125738.1:n.163+577_163+580del (NR2F2-AS1)
NM_001145155.2:c.43+31_43+34del (NR2F2) NP_001138627.1:n.43+31_43+34del
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