Canonical Allele Identifier: CA331787
Gene: NR2F1 HGNC NCBI

Linked Data

ClinVar Variation Id: 126493
ClinVar RCV Id: RCV000114387
dbSNP Id: rs587777274

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585367G>C , CM000667.2:g.93585367G>C GRCh38
NC_000005.9:g.92921073G>C , CM000667.1:g.92921073G>C GRCh37
NC_000005.8:g.92946829G>C NCBI36
NG_034119.1:g.7031G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.269G>C ENSP00000481517.1:p.Arg90Pro
ENST00000327111.8:c.344G>C MANE Select ENSP00000325819.3:p.Arg115Pro
ENST00000647447.1:c.191G>C ENSP00000495740.1:p.Arg64Pro
ENST00000327111.7:c.344G>C ENSP00000325819.3:p.Arg115Pro
ENST00000615873.1:c.269G>C ENSP00000481517.1:p.Arg90Pro
NM_005654.5:c.344G>C NP_005645.1:p.Arg115Pro
NM_005654.6:c.344G>C MANE Select NP_005645.1:p.Arg115Pro