Canonical Allele Identifier: CA1879991681
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800360C= , CM000671.2:g.127800360C= GRCh38
NC_000009.11:g.130562639C= , CM000671.1:g.130562639C= GRCh37
NC_000009.10:g.129602460C= NCBI36
NG_023245.1:g.2486C=

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3925C=
ENST00000479375.6:n.132-3925C=