Canonical Allele Identifier: CA2126000567
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1319138342
gnomAD v4: 14-28768843-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768843C>A , CM000676.2:g.28768843C>A GRCh38
NC_000014.8:g.29238049C>A , CM000676.1:g.29238049C>A GRCh37
NC_000014.7:g.28307800C>A NCBI36
NG_009367.1:g.6763C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*94C>A ENSP00000516406.1:n.*94C>A
ENST00000313071.7:c.*94C>A MANE Select ENSP00000339004.3:n.*94C>A
ENST00000313071.6:c.*94C>A ENSP00000339004.3:n.*94C>A
NM_005249.4:c.*94C>A NP_005240.3:n.*94C>A
NM_005249.5:c.*94C>A MANE Select NP_005240.3:n.*94C>A
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