Canonical Allele Identifier: CA613324883
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1339151174
gnomAD v2: 14-29238031-A-G
gnomAD v3: 14-28768825-A-G
gnomAD v4: 14-28768825-A-G
MyVariant Identifiers: chr14:g.29238031A>G (hg19) chr14:g.28768825A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768825A>G , CM000676.2:g.28768825A>G GRCh38
NC_000014.8:g.29238031A>G , CM000676.1:g.29238031A>G GRCh37
NC_000014.7:g.28307782A>G NCBI36
NG_009367.1:g.6745A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*76A>G ENSP00000516406.1:n.*76A>G
ENST00000313071.7:c.*76A>G MANE Select ENSP00000339004.3:n.*76A>G
ENST00000313071.6:c.*76A>G ENSP00000339004.3:n.*76A>G
NM_005249.4:c.*76A>G NP_005240.3:n.*76A>G
NM_005249.5:c.*76A>G MANE Select NP_005240.3:n.*76A>G
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