Canonical Allele Identifier: CA2801003474
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768818T>A , CM000676.2:g.28768818T>A GRCh38
NC_000014.8:g.29238024T>A , CM000676.1:g.29238024T>A GRCh37
NC_000014.7:g.28307775T>A NCBI36
NG_009367.1:g.6738T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*69T>A ENSP00000516406.1:n.*69T>A
ENST00000313071.7:c.*69T>A MANE Select ENSP00000339004.3:n.*69T>A
ENST00000313071.6:c.*69T>A ENSP00000339004.3:n.*69T>A
NM_005249.4:c.*69T>A NP_005240.3:n.*69T>A
NM_005249.5:c.*69T>A MANE Select NP_005240.3:n.*69T>A
Search 100 bp 5'
Search 100 bp 3'