Canonical Allele Identifier: CA961430585
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881830056
gnomAD v3: 14-28768770-A-T
gnomAD v4: 14-28768770-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768770A>T , CM000676.2:g.28768770A>T GRCh38
NC_000014.8:g.29237976A>T , CM000676.1:g.29237976A>T GRCh37
NC_000014.7:g.28307727A>T NCBI36
NG_009367.1:g.6690A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*21A>T ENSP00000516406.1:n.*21A>T
ENST00000313071.7:c.*21A>T MANE Select ENSP00000339004.3:n.*21A>T
ENST00000313071.6:c.*21A>T ENSP00000339004.3:n.*21A>T
NM_005249.4:c.*21A>T NP_005240.3:n.*21A>T
NM_005249.5:c.*21A>T MANE Select NP_005240.3:n.*21A>T
Search 100 bp 5'
Search 100 bp 3'