Canonical Allele Identifier: CA200280675
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs952849916

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800417A>G , CM000671.2:g.127800417A>G GRCh38
NC_000009.11:g.130562696A>G , CM000671.1:g.130562696A>G GRCh37
NC_000009.10:g.129602517A>G NCBI36
NG_023245.1:g.2543A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3868A>G
ENST00000479375.6:n.132-3868A>G