Canonical Allele Identifier: CA360526132

Gene: NR2F1

Linked Data

• MyVariant Identifiers: chr5:g.92921100C>G (hg19) ; chr5:g.93585394C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585394C>G , CM000667.2:g.93585394C>G	GRCh38
NC_000005.9:g.92921100C>G , CM000667.1:g.92921100C>G	GRCh37
NC_000005.8:g.92946856C>G	NCBI36
NG_034119.1:g.7058C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615873.2:c.296C>G	ENSP00000481517.1:p.Ala99Gly
ENST00000327111.8:c.371C>G MANE Select	ENSP00000325819.3:p.Ala124Gly
ENST00000647447.1:c.218C>G	ENSP00000495740.1:p.Ala73Gly
ENST00000327111.7:c.371C>G	ENSP00000325819.3:p.Ala124Gly
ENST00000615873.1:c.296C>G	ENSP00000481517.1:p.Ala99Gly
NM_005654.5:c.371C>G	NP_005645.1:p.Ala124Gly
NM_005654.6:c.371C>G MANE Select	NP_005645.1:p.Ala124Gly