Canonical Allele Identifier: CA123555
Gene: FOXG1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13871
ClinVar RCV Id: RCV000014885
dbSNP Id: rs267606827

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768203G>A , CM000676.2:g.28768203G>A GRCh38
NC_000014.8:g.29237409G>A , CM000676.1:g.29237409G>A GRCh37
NC_000014.7:g.28307160G>A NCBI36
NG_009367.1:g.6123G>A

Transcript Alleles

HGVS Amino-acid change
NM_005249.4:c.924G>A VV NP_005240.3:p.Trp308Ter
ENST00000313071.6:c.924G>A ENSP00000339004.3:p.Trp308Ter