Canonical Allele Identifier: CA389474765
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28767557-C-G
MyVariant Identifiers: chr14:g.29236763C>G (hg19) chr14:g.28767557C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767557C>G , CM000676.2:g.28767557C>G GRCh38
NC_000014.8:g.29236763C>G , CM000676.1:g.29236763C>G GRCh37
NC_000014.7:g.28306514C>G NCBI36
NG_009367.1:g.5477C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.278C>G ENSP00000516406.1:p.Ala93Gly
ENST00000313071.7:c.278C>G MANE Select ENSP00000339004.3:p.Ala93Gly
ENST00000313071.6:c.278C>G ENSP00000339004.3:p.Ala93Gly
NM_005249.4:c.278C>G NP_005240.3:p.Ala93Gly
NM_005249.5:c.278C>G MANE Select NP_005240.3:p.Ala93Gly
Search 100 bp 5'
Search 100 bp 3'