Canonical Allele Identifier: CA613324881
Gene: FOXG1 HGNC NCBI

Linked Data

dbSNP Id: rs1411250605
gnomAD v2: 14-29237975-T-G
gnomAD v4: 14-28768769-T-G
MyVariant Identifiers: chr14:g.29237975T>G (hg19) chr14:g.28768769T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768769T>G , CM000676.2:g.28768769T>G GRCh38
NC_000014.8:g.29237975T>G , CM000676.1:g.29237975T>G GRCh37
NC_000014.7:g.28307726T>G NCBI36
NG_009367.1:g.6689T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.*20T>G ENSP00000516406.1:n.*20T>G
ENST00000313071.7:c.*20T>G MANE Select ENSP00000339004.3:n.*20T>G
ENST00000313071.6:c.*20T>G ENSP00000339004.3:n.*20T>G
NM_005249.4:c.*20T>G NP_005240.3:n.*20T>G
NM_005249.5:c.*20T>G MANE Select NP_005240.3:n.*20T>G
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