Canonical Allele Identifier: CA1879991516
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800260A= , CM000671.2:g.127800260A= GRCh38
NC_000009.11:g.130562539A= , CM000671.1:g.130562539A= GRCh37
NC_000009.10:g.129602360A= NCBI36
NG_023245.1:g.2386A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-4025A=
ENST00000479375.6:n.132-4025A=