Canonical Allele Identifier: CA360526136

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92921102A>T (hg19) ; chr5:g.93585396A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585396A>T , CM000667.2:g.93585396A>T	GRCh38
NC_000005.9:g.92921102A>T , CM000667.1:g.92921102A>T	GRCh37
NC_000005.8:g.92946858A>T	NCBI36
NG_034119.1:g.7060A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.298A>T	ENSP00000481517.1:p.Asn100Tyr
ENST00000327111.8:c.373A>T MANE Select	ENSP00000325819.3:p.Asn125Tyr
ENST00000647447.1:c.220A>T	ENSP00000495740.1:p.Asn74Tyr
ENST00000327111.7:c.373A>T	ENSP00000325819.3:p.Asn125Tyr
ENST00000615873.1:c.298A>T	ENSP00000481517.1:p.Asn100Tyr
NM_005654.5:c.373A>T	NP_005645.1:p.Asn125Tyr
NM_005654.6:c.373A>T MANE Select	NP_005645.1:p.Asn125Tyr