Canonical Allele Identifier: CA1879991695

Gene: FPGS

Linked Data

• dbSNP Id: rs1829550492

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127800362G>C , CM000671.2:g.127800362G>C	GRCh38
NC_000009.11:g.130562641G>C , CM000671.1:g.130562641G>C	GRCh37
NC_000009.10:g.129602462G>C	NCBI36
NG_023245.1:g.2488G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479147.6:n.217-3923G>C
ENST00000479375.6:n.132-3923G>C