Canonical Allele Identifier: CA389474788
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 833617
ClinVar RCV Id: RCV001034081
dbSNP Id: rs1384097436
gnomAD v2: 14-29236772-A-G
gnomAD v3: 14-28767566-A-G
gnomAD v4: 14-28767566-A-G
MyVariant Identifiers: chr14:g.29236772A>G (hg19) chr14:g.28767566A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767566A>G , CM000676.2:g.28767566A>G GRCh38
NC_000014.8:g.29236772A>G , CM000676.1:g.29236772A>G GRCh37
NC_000014.7:g.28306523A>G NCBI36
NG_009367.1:g.5486A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.287A>G ENSP00000516406.1:p.Asp96Gly
ENST00000313071.7:c.287A>G MANE Select ENSP00000339004.3:p.Asp96Gly
ENST00000313071.6:c.287A>G ENSP00000339004.3:p.Asp96Gly
NM_005249.4:c.287A>G NP_005240.3:p.Asp96Gly
NM_005249.5:c.287A>G MANE Select NP_005240.3:p.Asp96Gly
Search 100 bp 5'
Search 100 bp 3'