Canonical Allele Identifier: CA389476092
Gene: FOXG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.29237381T>A (hg19) chr14:g.28768175T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768175T>A , CM000676.2:g.28768175T>A GRCh38
NC_000014.8:g.29237381T>A , CM000676.1:g.29237381T>A GRCh37
NC_000014.7:g.28307132T>A NCBI36
NG_009367.1:g.6095T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.896T>A ENSP00000516406.1:p.Phe299Tyr
ENST00000313071.7:c.896T>A MANE Select ENSP00000339004.3:p.Phe299Tyr
ENST00000313071.6:c.896T>A ENSP00000339004.3:p.Phe299Tyr
NM_005249.4:c.896T>A NP_005240.3:p.Phe299Tyr
NM_005249.5:c.896T>A MANE Select NP_005240.3:p.Phe299Tyr
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