Canonical Allele Identifier: CA389475173
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1911932
ClinVar RCV Id: RCV002578714 RCV003395493
MyVariant Identifiers: chr14:g.29236960G>A (hg19) chr14:g.28767754G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767754G>A , CM000676.2:g.28767754G>A GRCh38
NC_000014.8:g.29236960G>A , CM000676.1:g.29236960G>A GRCh37
NC_000014.7:g.28306711G>A NCBI36
NG_009367.1:g.5674G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.475G>A ENSP00000516406.1:p.Ala159Thr
ENST00000313071.7:c.475G>A MANE Select ENSP00000339004.3:p.Ala159Thr
ENST00000313071.6:c.475G>A ENSP00000339004.3:p.Ala159Thr
NM_005249.4:c.475G>A NP_005240.3:p.Ala159Thr
NM_005249.5:c.475G>A MANE Select NP_005240.3:p.Ala159Thr
Search 100 bp 5'
Search 100 bp 3'