Canonical Allele Identifier: CA2533356699
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768854A>C , CM000676.2:g.28768854A>C GRCh38
NC_000014.8:g.29238060A>C , CM000676.1:g.29238060A>C GRCh37
NC_000014.7:g.28307811A>C NCBI36
NG_009367.1:g.6774A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*105A>C ENSP00000516406.1:n.*105A>C
ENST00000313071.7:c.*105A>C MANE Select ENSP00000339004.3:n.*105A>C
ENST00000313071.6:c.*105A>C ENSP00000339004.3:n.*105A>C
NM_005249.4:c.*105A>C NP_005240.3:n.*105A>C
NM_005249.5:c.*105A>C MANE Select NP_005240.3:n.*105A>C
Search 100 bp 5'
Search 100 bp 3'