Canonical Allele Identifier: CA1879991673
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800353A= , CM000671.2:g.127800353A= GRCh38
NC_000009.11:g.130562632A= , CM000671.1:g.130562632A= GRCh37
NC_000009.10:g.129602453A= NCBI36
NG_023245.1:g.2479A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3932A=
ENST00000479375.6:n.132-3932A=