Canonical Allele Identifier: CA2126000303
Gene: FOXG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768156A= , CM000676.2:g.28768156A= GRCh38
NC_000014.8:g.29237362A= , CM000676.1:g.29237362A= GRCh37
NC_000014.7:g.28307113A= NCBI36
NG_009367.1:g.6076A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.877A= ENSP00000516406.1:p.Thr293=
ENST00000313071.7:c.877A= MANE Select ENSP00000339004.3:p.Thr293=
ENST00000313071.6:c.877A= ENSP00000339004.3:p.Thr293=
NM_005249.4:c.877A= NP_005240.3:p.Thr293=
NM_005249.5:c.877A= MANE Select NP_005240.3:p.Thr293=