Canonical Allele Identifier: CA389474344
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28767362-T-C
MyVariant Identifiers: chr14:g.29236568T>C (hg19) chr14:g.28767362T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767362T>C , CM000676.2:g.28767362T>C GRCh38
NC_000014.8:g.29236568T>C , CM000676.1:g.29236568T>C GRCh37
NC_000014.7:g.28306319T>C NCBI36
NG_009367.1:g.5282T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.83T>C ENSP00000516406.1:p.Val28Ala
ENST00000313071.7:c.83T>C MANE Select ENSP00000339004.3:p.Val28Ala
ENST00000313071.6:c.83T>C ENSP00000339004.3:p.Val28Ala
NM_005249.4:c.83T>C NP_005240.3:p.Val28Ala
NM_005249.5:c.83T>C MANE Select NP_005240.3:p.Val28Ala
Search 100 bp 5'
Search 100 bp 3'