Canonical Allele Identifier: CA314574
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205467
ClinVar RCV Id: RCV000187432 RCV000943970
dbSNP Id: rs796052451
gnomAD v2: 14-29236674-G-T
gnomAD v3: 14-28767468-G-T
gnomAD v4: 14-28767468-G-T
MyVariant Identifiers: chr14:g.29236674G>T (hg19) chr14:g.28767468G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767468G>T , CM000676.2:g.28767468G>T GRCh38
NC_000014.8:g.29236674G>T , CM000676.1:g.29236674G>T GRCh37
NC_000014.7:g.28306425G>T NCBI36
NG_009367.1:g.5388G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.189G>T ENSP00000516406.1:p.Pro63=
ENST00000313071.7:c.189G>T MANE Select ENSP00000339004.3:p.Pro63=
ENST00000313071.6:c.189G>T ENSP00000339004.3:p.Pro63=
NM_005249.4:c.189G>T NP_005240.3:p.Pro63=
NM_005249.5:c.189G>T MANE Select NP_005240.3:p.Pro63=
Search 100 bp 5'
Search 100 bp 3'