Canonical Allele Identifier: CA200280818
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs74585573

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800537G>A , CM000671.2:g.127800537G>A GRCh38
NC_000009.11:g.130562816G>A , CM000671.1:g.130562816G>A GRCh37
NC_000009.10:g.129602637G>A NCBI36
NG_023245.1:g.2663G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3748G>A
ENST00000479375.6:n.132-3748G>A