Canonical Allele Identifier: CA2430188897
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465706T= , CM000685.2:g.54465706T= GRCh38
NC_000023.10:g.54492139T= , CM000685.1:g.54492139T= GRCh37
NC_000023.9:g.54508864T= NCBI36
NG_008054.1:g.35461A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375135.4:c.1487A= MANE Select ENSP00000364277.3:p.His496=
ENST00000375135.3:c.1487A= ENSP00000364277.3:p.His496=
NM_004463.2:c.1487A= NP_004454.2:p.His496=
NM_004463.3:c.1487A= MANE Select NP_004454.2:p.His496=