Canonical Allele Identifier: CA860207647

Gene: FPGS

Linked Data

• dbSNP Id: rs1393733519
• MyVariant Identifiers: chr9:g.130562555G>T (hg19) ; chr9:g.127800276G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127800276G>T , CM000671.2:g.127800276G>T	GRCh38
NC_000009.11:g.130562555G>T , CM000671.1:g.130562555G>T	GRCh37
NC_000009.10:g.129602376G>T	NCBI36
NG_023245.1:g.2402G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479147.6:n.217-4009G>T
ENST00000479375.6:n.132-4009G>T