Canonical Allele Identifier: CA2575498216
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768808A>G , CM000676.2:g.28768808A>G GRCh38
NC_000014.8:g.29238014A>G , CM000676.1:g.29238014A>G GRCh37
NC_000014.7:g.28307765A>G NCBI36
NG_009367.1:g.6728A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*59A>G ENSP00000516406.1:n.*59A>G
ENST00000313071.7:c.*59A>G MANE Select ENSP00000339004.3:n.*59A>G
ENST00000313071.6:c.*59A>G ENSP00000339004.3:n.*59A>G
NM_005249.4:c.*59A>G NP_005240.3:n.*59A>G
NM_005249.5:c.*59A>G MANE Select NP_005240.3:n.*59A>G