Canonical Allele Identifier: CA2126000087
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768009C= , CM000676.2:g.28768009C= GRCh38
NC_000014.8:g.29237215C= , CM000676.1:g.29237215C= GRCh37
NC_000014.7:g.28306966C= NCBI36
NG_009367.1:g.5929C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.730C= ENSP00000516406.1:p.Arg244=
ENST00000313071.7:c.730C= MANE Select ENSP00000339004.3:p.Arg244=
ENST00000313071.6:c.730C= ENSP00000339004.3:p.Arg244=
NM_005249.4:c.730C= NP_005240.3:p.Arg244=
NM_005249.5:c.730C= MANE Select NP_005240.3:p.Arg244=