Canonical Allele Identifier: CA328946473
Gene: FGD1 HGNC NCBI

Linked Data

dbSNP Id: rs184454123
gnomAD v2: X-54521461-T-C
gnomAD v3: X-54495028-T-C
gnomAD v4: X-54495028-T-C
MyVariant Identifiers: chrX:g.54521461T>C (hg19) chrX:g.54495028T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495028T>C , CM000685.2:g.54495028T>C GRCh38
NC_000023.10:g.54521461T>C , CM000685.1:g.54521461T>C GRCh37
NC_000023.9:g.54538186T>C NCBI36
NG_008054.1:g.6139A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.307+98A>G MANE Select ENSP00000364277.3:n.307+98A>G
ENST00000375135.3:c.307+98A>G ENSP00000364277.3:n.307+98A>G
NM_004463.2:c.307+98A>G NP_004454.2:n.307+98A>G
NM_004463.3:c.307+98A>G MANE Select NP_004454.2:n.307+98A>G
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