Canonical Allele Identifier: CA1879991536

Gene: FPGS

Linked Data

• dbSNP Id: rs1829549897

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127800277G>T , CM000671.2:g.127800277G>T	GRCh38
NC_000009.11:g.130562556G>T , CM000671.1:g.130562556G>T	GRCh37
NC_000009.10:g.129602377G>T	NCBI36
NG_023245.1:g.2403G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479147.6:n.217-4008G>T
ENST00000479375.6:n.132-4008G>T