Canonical Allele Identifier: CA16606551
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 379912
dbSNP Id: rs1057520780

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767739G>T , CM000676.2:g.28767739G>T GRCh38
NC_000014.8:g.29236945G>T , CM000676.1:g.29236945G>T GRCh37
NC_000014.7:g.28306696G>T NCBI36
NG_009367.1:g.5659G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.460G>T ENSP00000516406.1:p.Glu154Ter
ENST00000313071.7:c.460G>T MANE Select ENSP00000339004.3:p.Glu154Ter
ENST00000313071.6:c.460G>T ENSP00000339004.3:p.Glu154Ter
NM_005249.4:c.460G>T NP_005240.3:p.Glu154Ter
NM_005249.5:c.460G>T MANE Select NP_005240.3:p.Glu154Ter