Canonical Allele Identifier: CA1879991652
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829550198

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800334_127800335del , CM000671.2:g.127800334_127800335del GRCh38
NC_000009.11:g.130562613_130562614del , CM000671.1:g.130562613_130562614del GRCh37
NC_000009.10:g.129602434_129602435del NCBI36
NG_023245.1:g.2460_2461del

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3951_217-3950del
ENST00000479375.6:n.132-3951_132-3950del