Canonical Allele Identifier: CA238810
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193306
dbSNP Id: rs760663911

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767497A>C , CM000676.2:g.28767497A>C GRCh38
NC_000014.8:g.29236703A>C , CM000676.1:g.29236703A>C GRCh37
NC_000014.7:g.28306454A>C NCBI36
NG_009367.1:g.5417A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.218A>C ENSP00000516406.1:p.Gln73Pro
ENST00000313071.7:c.218A>C MANE Select ENSP00000339004.3:p.Gln73Pro
ENST00000313071.6:c.218A>C ENSP00000339004.3:p.Gln73Pro
NM_005249.4:c.218A>C NP_005240.3:p.Gln73Pro
NM_005249.5:c.218A>C MANE Select NP_005240.3:p.Gln73Pro