Canonical Allele Identifier: CA360525892

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92920998G>T (hg19) ; chr5:g.93585292G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585292G>T , CM000667.2:g.93585292G>T	GRCh38
NC_000005.9:g.92920998G>T , CM000667.1:g.92920998G>T	GRCh37
NC_000005.8:g.92946754G>T	NCBI36
NG_034119.1:g.6956G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.194G>T	ENSP00000481517.1:p.Gly65Val
ENST00000327111.8:c.269G>T MANE Select	ENSP00000325819.3:p.Gly90Val
ENST00000647447.1:c.116G>T	ENSP00000495740.1:p.Gly39Val
ENST00000327111.7:c.269G>T	ENSP00000325819.3:p.Gly90Val
ENST00000615873.1:c.194G>T	ENSP00000481517.1:p.Gly65Val
NM_005654.5:c.269G>T	NP_005645.1:p.Gly90Val
NM_005654.6:c.269G>T MANE Select	NP_005645.1:p.Gly90Val