Canonical Allele Identifier: CA258396610
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs972261580
gnomAD v3: 14-28768821-G-A
gnomAD v4: 14-28768821-G-A
MyVariant Identifiers: chr14:g.29238027G>A (hg19) chr14:g.28768821G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768821G>A , CM000676.2:g.28768821G>A GRCh38
NC_000014.8:g.29238027G>A , CM000676.1:g.29238027G>A GRCh37
NC_000014.7:g.28307778G>A NCBI36
NG_009367.1:g.6741G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*72G>A ENSP00000516406.1:n.*72G>A
ENST00000313071.7:c.*72G>A MANE Select ENSP00000339004.3:n.*72G>A
ENST00000313071.6:c.*72G>A ENSP00000339004.3:n.*72G>A
NM_005249.4:c.*72G>A NP_005240.3:n.*72G>A
NM_005249.5:c.*72G>A MANE Select NP_005240.3:n.*72G>A
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