Canonical Allele Identifier: CA389476034
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768145G>T , CM000676.2:g.28768145G>T GRCh38
NC_000014.8:g.29237351G>T , CM000676.1:g.29237351G>T GRCh37
NC_000014.7:g.28307102G>T NCBI36
NG_009367.1:g.6065G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.866G>T ENSP00000516406.1:p.Gly289Val
ENST00000313071.7:c.866G>T MANE Select ENSP00000339004.3:p.Gly289Val
ENST00000313071.6:c.866G>T ENSP00000339004.3:p.Gly289Val
NM_005249.4:c.866G>T NP_005240.3:p.Gly289Val
NM_005249.5:c.866G>T MANE Select NP_005240.3:p.Gly289Val