Canonical Allele Identifier: CA445722151

Gene: NR2F1

Linked Data

• dbSNP Id: rs1349953924
• gnomAD v3: 5-93585293-G-T
• gnomAD v4: 5-93585293-G-T
• MyVariant Identifiers: chr5:g.92920999G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585293G>T , CM000667.2:g.93585293G>T	GRCh38
NC_000005.9:g.92920999G>T , CM000667.1:g.92920999G>T	GRCh37
NC_000005.8:g.92946755G>T	NCBI36
NG_034119.1:g.6957G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.195G>T	ENSP00000481517.1:p.Gly65=
ENST00000327111.8:c.270G>T MANE Select	ENSP00000325819.3:p.Gly90=
ENST00000647447.1:c.117G>T	ENSP00000495740.1:p.Gly39=
ENST00000327111.7:c.270G>T	ENSP00000325819.3:p.Gly90=
ENST00000615873.1:c.195G>T	ENSP00000481517.1:p.Gly65=
NM_005654.5:c.270G>T	NP_005645.1:p.Gly90=
NM_005654.6:c.270G>T MANE Select	NP_005645.1:p.Gly90=