Canonical Allele Identifier: CA961430587
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs756488909
gnomAD v3: 14-28768774-GA-G
gnomAD v4: 14-28768774-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768776del , CM000676.2:g.28768776del GRCh38
NC_000014.8:g.29237982del , CM000676.1:g.29237982del GRCh37
NC_000014.7:g.28307733del NCBI36
NG_009367.1:g.6696del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*27del ENSP00000516406.1:n.*27del
ENST00000313071.7:c.*27del MANE Select ENSP00000339004.3:n.*27del
ENST00000313071.6:c.*27del ENSP00000339004.3:n.*27del
NM_005249.4:c.*27del NP_005240.3:n.*27del
NM_005249.5:c.*27del MANE Select NP_005240.3:n.*27del
Search 100 bp 5'
Search 100 bp 3'