Canonical Allele Identifier: CA2729377189
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs2138662531
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768829A>C , CM000676.2:g.28768829A>C GRCh38
NC_000014.8:g.29238035A>C , CM000676.1:g.29238035A>C GRCh37
NC_000014.7:g.28307786A>C NCBI36
NG_009367.1:g.6749A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*80A>C ENSP00000516406.1:n.*80A>C
ENST00000313071.7:c.*80A>C MANE Select ENSP00000339004.3:n.*80A>C
ENST00000313071.6:c.*80A>C ENSP00000339004.3:n.*80A>C
NM_005249.4:c.*80A>C NP_005240.3:n.*80A>C
NM_005249.5:c.*80A>C MANE Select NP_005240.3:n.*80A>C
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