Canonical Allele Identifier: CA445569994

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92921101C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585395C>T , CM000667.2:g.93585395C>T	GRCh38
NC_000005.9:g.92921101C>T , CM000667.1:g.92921101C>T	GRCh37
NC_000005.8:g.92946857C>T	NCBI36
NG_034119.1:g.7059C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.297C>T	ENSP00000481517.1:p.Ala99=
ENST00000327111.8:c.372C>T MANE Select	ENSP00000325819.3:p.Ala124=
ENST00000647447.1:c.219C>T	ENSP00000495740.1:p.Ala73=
ENST00000327111.7:c.372C>T	ENSP00000325819.3:p.Ala124=
ENST00000615873.1:c.297C>T	ENSP00000481517.1:p.Ala99=
NM_005654.5:c.372C>T	NP_005645.1:p.Ala124=
NM_005654.6:c.372C>T MANE Select	NP_005645.1:p.Ala124=