Canonical Allele Identifier: CA389474732
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 588146
ClinVar RCV Id: RCV002316066 RCV002533003
dbSNP Id: rs1566445056
MyVariant Identifiers: chr14:g.29236744A>C (hg19) chr14:g.28767538A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767538A>C , CM000676.2:g.28767538A>C GRCh38
NC_000014.8:g.29236744A>C , CM000676.1:g.29236744A>C GRCh37
NC_000014.7:g.28306495A>C NCBI36
NG_009367.1:g.5458A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.259A>C ENSP00000516406.1:p.Thr87Pro
ENST00000313071.7:c.259A>C MANE Select ENSP00000339004.3:p.Thr87Pro
ENST00000313071.6:c.259A>C ENSP00000339004.3:p.Thr87Pro
NM_005249.4:c.259A>C NP_005240.3:p.Thr87Pro
NM_005249.5:c.259A>C MANE Select NP_005240.3:p.Thr87Pro
Search 100 bp 5'
Search 100 bp 3'