Canonical Allele Identifier: CA655705540
Gene: FOXG1 HGNC NCBI

Linked Data

COSMIC: COSN21209908
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768796T>C , CM000676.2:g.28768796T>C GRCh38
NC_000014.8:g.29238002T>C , CM000676.1:g.29238002T>C GRCh37
NC_000014.7:g.28307753T>C NCBI36
NG_009367.1:g.6716T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*47T>C ENSP00000516406.1:n.*47T>C
ENST00000313071.7:c.*47T>C MANE Select ENSP00000339004.3:n.*47T>C
ENST00000313071.6:c.*47T>C ENSP00000339004.3:n.*47T>C
NM_005249.4:c.*47T>C NP_005240.3:n.*47T>C
NM_005249.5:c.*47T>C MANE Select NP_005240.3:n.*47T>C
Search 100 bp 5'
Search 100 bp 3'