Canonical Allele Identifier: CA389477192
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920894
ClinVar RCV Id: RCV002591325
gnomAD v4: 14-28768685-G-T
MyVariant Identifiers: chr14:g.29237891G>T (hg19) chr14:g.28768685G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768685G>T , CM000676.2:g.28768685G>T GRCh38
NC_000014.8:g.29237891G>T , CM000676.1:g.29237891G>T GRCh37
NC_000014.7:g.28307642G>T NCBI36
NG_009367.1:g.6605G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.1406G>T ENSP00000516406.1:p.Gly469Val
ENST00000313071.7:c.1406G>T MANE Select ENSP00000339004.3:p.Gly469Val
ENST00000313071.6:c.1406G>T ENSP00000339004.3:p.Gly469Val
NM_005249.4:c.1406G>T NP_005240.3:p.Gly469Val
NM_005249.5:c.1406G>T MANE Select NP_005240.3:p.Gly469Val
Search 100 bp 5'
Search 100 bp 3'