Canonical Allele Identifier: CA360526147

Gene: NR2F1

Linked Data

• gnomAD v4: 5-93585401-G-T
• MyVariant Identifiers: chr5:g.92921107G>T (hg19) ; chr5:g.93585401G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585401G>T , CM000667.2:g.93585401G>T	GRCh38
NC_000005.9:g.92921107G>T , CM000667.1:g.92921107G>T	GRCh37
NC_000005.8:g.92946863G>T	NCBI36
NG_034119.1:g.7065G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.303G>T	ENSP00000481517.1:p.Arg101Ser
ENST00000327111.8:c.378G>T MANE Select	ENSP00000325819.3:p.Arg126Ser
ENST00000647447.1:c.225G>T	ENSP00000495740.1:p.Arg75Ser
ENST00000327111.7:c.378G>T	ENSP00000325819.3:p.Arg126Ser
ENST00000615873.1:c.303G>T	ENSP00000481517.1:p.Arg101Ser
NM_005654.5:c.378G>T	NP_005645.1:p.Arg126Ser
NM_005654.6:c.378G>T MANE Select	NP_005645.1:p.Arg126Ser