Canonical Allele Identifier: CA860207665

Gene: FPGS

Linked Data

• dbSNP Id: rs1455104228
• MyVariant Identifiers: chr9:g.130562581G>A (hg19) ; chr9:g.127800302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127800302G>A , CM000671.2:g.127800302G>A	GRCh38
NC_000009.11:g.130562581G>A , CM000671.1:g.130562581G>A	GRCh37
NC_000009.10:g.129602402G>A	NCBI36
NG_023245.1:g.2428G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479147.6:n.217-3983G>A
ENST00000479375.6:n.132-3983G>A