Canonical Allele Identifier: CA1879991914
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800491T= , CM000671.2:g.127800491T= GRCh38
NC_000009.11:g.130562770T= , CM000671.1:g.130562770T= GRCh37
NC_000009.10:g.129602591T= NCBI36
NG_023245.1:g.2617T=

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3794T=
ENST00000479375.6:n.132-3794T=