Canonical Allele Identifier: CA704725682
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1186068607
gnomAD v3: 14-28768810-T-C
gnomAD v4: 14-28768810-T-C
MyVariant Identifiers: chr14:g.29238016T>C (hg19) chr14:g.28768810T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768810T>C , CM000676.2:g.28768810T>C GRCh38
NC_000014.8:g.29238016T>C , CM000676.1:g.29238016T>C GRCh37
NC_000014.7:g.28307767T>C NCBI36
NG_009367.1:g.6730T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*61T>C ENSP00000516406.1:n.*61T>C
ENST00000313071.7:c.*61T>C MANE Select ENSP00000339004.3:n.*61T>C
ENST00000313071.6:c.*61T>C ENSP00000339004.3:n.*61T>C
NM_005249.4:c.*61T>C NP_005240.3:n.*61T>C
NM_005249.5:c.*61T>C MANE Select NP_005240.3:n.*61T>C
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