Canonical Allele Identifier: CA1879991520
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829549857

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800263_127800264del , CM000671.2:g.127800263_127800264del GRCh38
NC_000009.11:g.130562542_130562543del , CM000671.1:g.130562542_130562543del GRCh37
NC_000009.10:g.129602363_129602364del NCBI36
NG_023245.1:g.2389_2390del

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-4022_217-4021del
ENST00000479375.6:n.132-4022_132-4021del