Canonical Allele Identifier: CA613324879
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1171678086
gnomAD v2: 14-29237971-A-C
gnomAD v3: 14-28768765-A-C
gnomAD v4: 14-28768765-A-C
MyVariant Identifiers: chr14:g.29237971A>C (hg19) chr14:g.28768765A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768765A>C , CM000676.2:g.28768765A>C GRCh38
NC_000014.8:g.29237971A>C , CM000676.1:g.29237971A>C GRCh37
NC_000014.7:g.28307722A>C NCBI36
NG_009367.1:g.6685A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*16A>C ENSP00000516406.1:n.*16A>C
ENST00000313071.7:c.*16A>C MANE Select ENSP00000339004.3:n.*16A>C
ENST00000313071.6:c.*16A>C ENSP00000339004.3:n.*16A>C
NM_005249.4:c.*16A>C NP_005240.3:n.*16A>C
NM_005249.5:c.*16A>C MANE Select NP_005240.3:n.*16A>C
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