Canonical Allele Identifier: CA1129265427
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829551646

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800463del , CM000671.2:g.127800463del GRCh38
NC_000009.11:g.130562742del , CM000671.1:g.130562742del GRCh37
NC_000009.10:g.129602563del NCBI36
NG_023245.1:g.2589del

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3822del
ENST00000479375.6:n.132-3822del