Canonical Allele Identifier: CA2838760077
Gene: FPGS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800467G>A , CM000671.2:g.127800467G>A GRCh38
NC_000009.11:g.130562746G>A , CM000671.1:g.130562746G>A GRCh37
NC_000009.10:g.129602567G>A NCBI36
NG_023245.1:g.2593G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3818G>A
ENST00000479375.6:n.132-3818G>A
Search 100 bp 5'
Search 100 bp 3'