Canonical Allele Identifier: CA1879991717
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800387_127800388delinsTC , CM000671.2:g.127800387_127800388delinsTC GRCh38
NC_000009.11:g.130562666_130562667delinsTC , CM000671.1:g.130562666_130562667delinsTC GRCh37
NC_000009.10:g.129602487_129602488delinsTC NCBI36
NG_023245.1:g.2513_2514delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3898_217-3897delinsTC
ENST00000479375.6:n.132-3898_132-3897delinsTC