Canonical Allele Identifier: CA1879991899

Gene: FPGS

Linked Data

• dbSNP Id: rs1288017026

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127800472A>C , CM000671.2:g.127800472A>C	GRCh38
NC_000009.11:g.130562751A>C , CM000671.1:g.130562751A>C	GRCh37
NC_000009.10:g.129602572A>C	NCBI36
NG_023245.1:g.2598A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479147.6:n.217-3813A>C
ENST00000479375.6:n.132-3813A>C