Canonical Allele Identifier: CA1879991834
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800445A= , CM000671.2:g.127800445A= GRCh38
NC_000009.11:g.130562724A= , CM000671.1:g.130562724A= GRCh37
NC_000009.10:g.129602545A= NCBI36
NG_023245.1:g.2571A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3840A=
ENST00000479375.6:n.132-3840A=