Canonical Allele Identifier: CA2839958935
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800400C>A , CM000671.2:g.127800400C>A GRCh38
NC_000009.11:g.130562679C>A , CM000671.1:g.130562679C>A GRCh37
NC_000009.10:g.129602500C>A NCBI36
NG_023245.1:g.2526C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3885C>A
ENST00000479375.6:n.132-3885C>A