Canonical Allele Identifier: CA704725678
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1423966561
gnomAD v3: 14-28768805-A-C
gnomAD v4: 14-28768805-A-C
MyVariant Identifiers: chr14:g.29238011A>C (hg19) chr14:g.28768805A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768805A>C , CM000676.2:g.28768805A>C GRCh38
NC_000014.8:g.29238011A>C , CM000676.1:g.29238011A>C GRCh37
NC_000014.7:g.28307762A>C NCBI36
NG_009367.1:g.6725A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*56A>C ENSP00000516406.1:n.*56A>C
ENST00000313071.7:c.*56A>C MANE Select ENSP00000339004.3:n.*56A>C
ENST00000313071.6:c.*56A>C ENSP00000339004.3:n.*56A>C
NM_005249.4:c.*56A>C NP_005240.3:n.*56A>C
NM_005249.5:c.*56A>C MANE Select NP_005240.3:n.*56A>C
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