Canonical Allele Identifier: CA2125999967
Gene: FOXG1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767958A= , CM000676.2:g.28767958A= GRCh38
NC_000014.8:g.29237164A= , CM000676.1:g.29237164A= GRCh37
NC_000014.7:g.28306915A= NCBI36
NG_009367.1:g.5878A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.679A= ENSP00000516406.1:p.Asn227=
ENST00000313071.7:c.679A= MANE Select ENSP00000339004.3:p.Asn227=
ENST00000313071.6:c.679A= ENSP00000339004.3:p.Asn227=
NM_005249.4:c.679A= NP_005240.3:p.Asn227=
NM_005249.5:c.679A= MANE Select NP_005240.3:p.Asn227=
Search 100 bp 5'
Search 100 bp 3'