Canonical Allele Identifier: CA393929931
Gene: NR2F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.96875585A>G (hg19) chr15:g.96332356A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96332356A>G , CM000677.2:g.96332356A>G GRCh38
NC_000015.9:g.96875585A>G , CM000677.1:g.96875585A>G GRCh37
NC_000015.8:g.94676589A>G NCBI36
NG_016753.1:g.11429A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000394166.8:c.251A>G MANE Select ENSP00000377721.3:p.Asp84Gly
ENST00000394166.7:c.251A>G ENSP00000377721.3:p.Asp84Gly
ENST00000421109.6:c.44-1720A>G ENSP00000401674.2:n.44-1720A>G
NM_001145155.1:c.44-1720A>G NP_001138627.1:n.44-1720A>G
NM_021005.3:c.251A>G NP_066285.1:p.Asp84Gly
NM_021005.4:c.251A>G MANE Select NP_066285.1:p.Asp84Gly
NM_001145155.2:c.44-1720A>G NP_001138627.1:n.44-1720A>G
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