Canonical Allele Identifier: CA1129265418
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1588543894

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800422A>G , CM000671.2:g.127800422A>G GRCh38
NC_000009.11:g.130562701A>G , CM000671.1:g.130562701A>G GRCh37
NC_000009.10:g.129602522A>G NCBI36
NG_023245.1:g.2548A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3863A>G
ENST00000479375.6:n.132-3863A>G