Canonical Allele Identifier: CA314648
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205507
ClinVar RCV Id: RCV000187483
dbSNP Id: rs796052481

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767950G>A , CM000676.2:g.28767950G>A GRCh38
NC_000014.8:g.29237156G>A , CM000676.1:g.29237156G>A GRCh37
NC_000014.7:g.28306907G>A NCBI36
NG_009367.1:g.5870G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.671G>A ENSP00000516406.1:p.Gly224Asp
ENST00000313071.7:c.671G>A MANE Select ENSP00000339004.3:p.Gly224Asp
ENST00000313071.6:c.671G>A ENSP00000339004.3:p.Gly224Asp
NM_005249.4:c.671G>A NP_005240.3:p.Gly224Asp
NM_005249.5:c.671G>A MANE Select NP_005240.3:p.Gly224Asp