Canonical Allele Identifier: CA360525889

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92920997G>T (hg19) ; chr5:g.93585291G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585291G>T , CM000667.2:g.93585291G>T	GRCh38
NC_000005.9:g.92920997G>T , CM000667.1:g.92920997G>T	GRCh37
NC_000005.8:g.92946753G>T	NCBI36
NG_034119.1:g.6955G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.193G>T	ENSP00000481517.1:p.Gly65Trp
ENST00000327111.8:c.268G>T MANE Select	ENSP00000325819.3:p.Gly90Trp
ENST00000647447.1:c.115G>T	ENSP00000495740.1:p.Gly39Trp
ENST00000327111.7:c.268G>T	ENSP00000325819.3:p.Gly90Trp
ENST00000615873.1:c.193G>T	ENSP00000481517.1:p.Gly65Trp
NM_005654.5:c.268G>T	NP_005645.1:p.Gly90Trp
NM_005654.6:c.268G>T MANE Select	NP_005645.1:p.Gly90Trp