Canonical Allele Identifier: CA445569987

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92921095C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585389C>T , CM000667.2:g.93585389C>T	GRCh38
NC_000005.9:g.92921095C>T , CM000667.1:g.92921095C>T	GRCh37
NC_000005.8:g.92946851C>T	NCBI36
NG_034119.1:g.7053C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.291C>T	ENSP00000481517.1:p.Cys97=
ENST00000327111.8:c.366C>T MANE Select	ENSP00000325819.3:p.Cys122=
ENST00000647447.1:c.213C>T	ENSP00000495740.1:p.Cys71=
ENST00000327111.7:c.366C>T	ENSP00000325819.3:p.Cys122=
ENST00000615873.1:c.291C>T	ENSP00000481517.1:p.Cys97=
NM_005654.5:c.366C>T	NP_005645.1:p.Cys122=
NM_005654.6:c.366C>T MANE Select	NP_005645.1:p.Cys122=