Canonical Allele Identifier: CA486098736
Gene: FOXG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.29237826C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768620C>A , CM000676.2:g.28768620C>A GRCh38
NC_000014.8:g.29237826C>A , CM000676.1:g.29237826C>A GRCh37
NC_000014.7:g.28307577C>A NCBI36
NG_009367.1:g.6540C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.1341C>A ENSP00000516406.1:p.Ala447=
ENST00000313071.7:c.1341C>A MANE Select ENSP00000339004.3:p.Ala447=
ENST00000313071.6:c.1341C>A ENSP00000339004.3:p.Ala447=
NM_005249.4:c.1341C>A NP_005240.3:p.Ala447=
NM_005249.5:c.1341C>A MANE Select NP_005240.3:p.Ala447=
Search 100 bp 5'
Search 100 bp 3'