Canonical Allele Identifier: CA1879991540
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800278T= , CM000671.2:g.127800278T= GRCh38
NC_000009.11:g.130562557T= , CM000671.1:g.130562557T= GRCh37
NC_000009.10:g.129602378T= NCBI36
NG_023245.1:g.2404T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-4007T=
ENST00000479375.6:n.132-4007T=