Canonical Allele Identifier: CA2126000579
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1881832042
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768852C>T , CM000676.2:g.28768852C>T GRCh38
NC_000014.8:g.29238058C>T , CM000676.1:g.29238058C>T GRCh37
NC_000014.7:g.28307809C>T NCBI36
NG_009367.1:g.6772C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*103C>T ENSP00000516406.1:n.*103C>T
ENST00000313071.7:c.*103C>T MANE Select ENSP00000339004.3:n.*103C>T
ENST00000313071.6:c.*103C>T ENSP00000339004.3:n.*103C>T
NM_005249.4:c.*103C>T NP_005240.3:n.*103C>T
NM_005249.5:c.*103C>T MANE Select NP_005240.3:n.*103C>T
Search 100 bp 5'
Search 100 bp 3'