Canonical Allele Identifier: CA1879991855
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800453G= , CM000671.2:g.127800453G= GRCh38
NC_000009.11:g.130562732G= , CM000671.1:g.130562732G= GRCh37
NC_000009.10:g.129602553G= NCBI36
NG_023245.1:g.2579G=

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3832G=
ENST00000479375.6:n.132-3832G=