Canonical Allele Identifier: CA1879991751
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800406C= , CM000671.2:g.127800406C= GRCh38
NC_000009.11:g.130562685C= , CM000671.1:g.130562685C= GRCh37
NC_000009.10:g.129602506C= NCBI36
NG_023245.1:g.2532C=

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3879C=
ENST00000479375.6:n.132-3879C=