Canonical Allele Identifier: CA200280583

Gene: FPGS

Linked Data

• dbSNP Id: rs774888878
• MyVariant Identifiers: chr9:g.130562632A>G (hg19) ; chr9:g.127800353A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127800353A>G , CM000671.2:g.127800353A>G	GRCh38
NC_000009.11:g.130562632A>G , CM000671.1:g.130562632A>G	GRCh37
NC_000009.10:g.129602453A>G	NCBI36
NG_023245.1:g.2479A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479147.6:n.217-3932A>G
ENST00000479375.6:n.132-3932A>G