Canonical Allele Identifier: CA389474480
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881777867
gnomAD v4: 14-28767420-C-G
MyVariant Identifiers: chr14:g.29236626C>G (hg19) chr14:g.28767420C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767420C>G , CM000676.2:g.28767420C>G GRCh38
NC_000014.8:g.29236626C>G , CM000676.1:g.29236626C>G GRCh37
NC_000014.7:g.28306377C>G NCBI36
NG_009367.1:g.5340C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.141C>G ENSP00000516406.1:p.His47Gln
ENST00000313071.7:c.141C>G MANE Select ENSP00000339004.3:p.His47Gln
ENST00000313071.6:c.141C>G ENSP00000339004.3:p.His47Gln
NM_005249.4:c.141C>G NP_005240.3:p.His47Gln
NM_005249.5:c.141C>G MANE Select NP_005240.3:p.His47Gln
Search 100 bp 5'
Search 100 bp 3'