Canonical Allele Identifier: CA2624400769
Gene: FOXG1 HGNC NCBI

Linked Data

gnomAD v4: 14-28768846-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768846C>T , CM000676.2:g.28768846C>T GRCh38
NC_000014.8:g.29238052C>T , CM000676.1:g.29238052C>T GRCh37
NC_000014.7:g.28307803C>T NCBI36
NG_009367.1:g.6766C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*97C>T ENSP00000516406.1:n.*97C>T
ENST00000313071.7:c.*97C>T MANE Select ENSP00000339004.3:n.*97C>T
ENST00000313071.6:c.*97C>T ENSP00000339004.3:n.*97C>T
NM_005249.4:c.*97C>T NP_005240.3:n.*97C>T
NM_005249.5:c.*97C>T MANE Select NP_005240.3:n.*97C>T
Search 100 bp 5'
Search 100 bp 3'