Canonical Allele Identifier: CA1879991941
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800506G= , CM000671.2:g.127800506G= GRCh38
NC_000009.11:g.130562785G= , CM000671.1:g.130562785G= GRCh37
NC_000009.10:g.129602606G= NCBI36
NG_023245.1:g.2632G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3779G=
ENST00000479375.6:n.132-3779G=