Canonical Allele Identifier: CA1879991773
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829551183

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800427dup , CM000671.2:g.127800427dup GRCh38
NC_000009.11:g.130562706dup , CM000671.1:g.130562706dup GRCh37
NC_000009.10:g.129602527dup NCBI36
NG_023245.1:g.2553dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3858dup
ENST00000479375.6:n.132-3858dup