Canonical Allele Identifier: CA1129265432
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829551826

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800490A>G , CM000671.2:g.127800490A>G GRCh38
NC_000009.11:g.130562769A>G , CM000671.1:g.130562769A>G GRCh37
NC_000009.10:g.129602590A>G NCBI36
NG_023245.1:g.2616A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3795A>G
ENST00000479375.6:n.132-3795A>G