Canonical Allele Identifier: CA445722150
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs1349953924
gnomAD v3: 5-93585293-G-C
gnomAD v4: 5-93585293-G-C

Genomic Alleles

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

Transcript Alleles

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