Canonical Allele Identifier: CA961430595
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881830830

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768813A>T , CM000676.2:g.28768813A>T GRCh38
NC_000014.8:g.29238019A>T , CM000676.1:g.29238019A>T GRCh37
NC_000014.7:g.28307770A>T NCBI36
NG_009367.1:g.6733A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*64A>T ENSP00000516406.1:n.*64A>T
ENST00000313071.7:c.*64A>T MANE Select ENSP00000339004.3:n.*64A>T
ENST00000313071.6:c.*64A>T ENSP00000339004.3:n.*64A>T
NM_005249.4:c.*64A>T NP_005240.3:n.*64A>T
NM_005249.5:c.*64A>T MANE Select NP_005240.3:n.*64A>T