Canonical Allele Identifier: CA516689349
Gene: FGD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.54492132C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465699C>T , CM000685.2:g.54465699C>T GRCh38
NC_000023.10:g.54492132C>T , CM000685.1:g.54492132C>T GRCh37
NC_000023.9:g.54508857C>T NCBI36
NG_008054.1:g.35468G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375135.4:c.1494G>A MANE Select ENSP00000364277.3:p.Val498=
ENST00000375135.3:c.1494G>A ENSP00000364277.3:p.Val498=
NM_004463.2:c.1494G>A NP_004454.2:p.Val498=
NM_004463.3:c.1494G>A MANE Select NP_004454.2:p.Val498=
Search 100 bp 5'
Search 100 bp 3'