Canonical Allele Identifier: CA2126000378
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768341C= , CM000676.2:g.28768341C= GRCh38
NC_000014.8:g.29237547C= , CM000676.1:g.29237547C= GRCh37
NC_000014.7:g.28307298C= NCBI36
NG_009367.1:g.6261C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.1062C= ENSP00000516406.1:p.His354=
ENST00000313071.7:c.1062C= MANE Select ENSP00000339004.3:p.His354=
ENST00000313071.6:c.1062C= ENSP00000339004.3:p.His354=
NM_005249.4:c.1062C= NP_005240.3:p.His354=
NM_005249.5:c.1062C= MANE Select NP_005240.3:p.His354=