Canonical Allele Identifier: CA389476863
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881823142

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768532T>C , CM000676.2:g.28768532T>C GRCh38
NC_000014.8:g.29237738T>C , CM000676.1:g.29237738T>C GRCh37
NC_000014.7:g.28307489T>C NCBI36
NG_009367.1:g.6452T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.1253T>C ENSP00000516406.1:p.Phe418Ser
ENST00000313071.7:c.1253T>C MANE Select ENSP00000339004.3:p.Phe418Ser
ENST00000313071.6:c.1253T>C ENSP00000339004.3:p.Phe418Ser
NM_005249.4:c.1253T>C NP_005240.3:p.Phe418Ser
NM_005249.5:c.1253T>C MANE Select NP_005240.3:p.Phe418Ser