Canonical Allele Identifier: CA389475732
Gene: FOXG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.29237210T>C (hg19) chr14:g.28768004T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768004T>C , CM000676.2:g.28768004T>C GRCh38
NC_000014.8:g.29237210T>C , CM000676.1:g.29237210T>C GRCh37
NC_000014.7:g.28306961T>C NCBI36
NG_009367.1:g.5924T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.725T>C ENSP00000516406.1:p.Val242Ala
ENST00000313071.7:c.725T>C MANE Select ENSP00000339004.3:p.Val242Ala
ENST00000313071.6:c.725T>C ENSP00000339004.3:p.Val242Ala
NM_005249.4:c.725T>C NP_005240.3:p.Val242Ala
NM_005249.5:c.725T>C MANE Select NP_005240.3:p.Val242Ala
Search 100 bp 5'
Search 100 bp 3'