Canonical Allele Identifier: CA360525902

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92921003A>T (hg19) ; chr5:g.93585297A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585297A>T , CM000667.2:g.93585297A>T	GRCh38
NC_000005.9:g.92921003A>T , CM000667.1:g.92921003A>T	GRCh37
NC_000005.8:g.92946759A>T	NCBI36
NG_034119.1:g.6961A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.199A>T	ENSP00000481517.1:p.Lys67Ter
ENST00000327111.8:c.274A>T MANE Select	ENSP00000325819.3:p.Lys92Ter
ENST00000647447.1:c.121A>T	ENSP00000495740.1:p.Lys41Ter
ENST00000327111.7:c.274A>T	ENSP00000325819.3:p.Lys92Ter
ENST00000615873.1:c.199A>T	ENSP00000481517.1:p.Lys67Ter
NM_005654.5:c.274A>T	NP_005645.1:p.Lys92Ter
NM_005654.6:c.274A>T MANE Select	NP_005645.1:p.Lys92Ter