Canonical Allele Identifier: CA486098376
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1392520466

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768449C>T , CM000676.2:g.28768449C>T GRCh38
NC_000014.8:g.29237655C>T , CM000676.1:g.29237655C>T GRCh37
NC_000014.7:g.28307406C>T NCBI36
NG_009367.1:g.6369C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706482.1:c.1170C>T ENSP00000516406.1:p.Cys390=
ENST00000313071.7:c.1170C>T MANE Select ENSP00000339004.3:p.Cys390=
ENST00000313071.6:c.1170C>T ENSP00000339004.3:p.Cys390=
NM_005249.4:c.1170C>T NP_005240.3:p.Cys390=
NM_005249.5:c.1170C>T MANE Select NP_005240.3:p.Cys390=