Canonical Allele Identifier: CA360525899

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92921002C>A (hg19) ; chr5:g.93585296C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585296C>A , CM000667.2:g.93585296C>A	GRCh38
NC_000005.9:g.92921002C>A , CM000667.1:g.92921002C>A	GRCh37
NC_000005.8:g.92946758C>A	NCBI36
NG_034119.1:g.6960C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615873.2:c.198C>A	ENSP00000481517.1:p.Asp66Glu
ENST00000327111.8:c.273C>A MANE Select	ENSP00000325819.3:p.Asp91Glu
ENST00000647447.1:c.120C>A	ENSP00000495740.1:p.Asp40Glu
ENST00000327111.7:c.273C>A	ENSP00000325819.3:p.Asp91Glu
ENST00000615873.1:c.198C>A	ENSP00000481517.1:p.Asp66Glu
NM_005654.5:c.273C>A	NP_005645.1:p.Asp91Glu
NM_005654.6:c.273C>A MANE Select	NP_005645.1:p.Asp91Glu