Canonical Allele Identifier: CA1879991670
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829550340

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800353_127800354del , CM000671.2:g.127800353_127800354del GRCh38
NC_000009.11:g.130562632_130562633del , CM000671.1:g.130562632_130562633del GRCh37
NC_000009.10:g.129602453_129602454del NCBI36
NG_023245.1:g.2479_2480del

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3932_217-3931del
ENST00000479375.6:n.132-3932_132-3931del