Canonical Allele Identifier: CA2580574805
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800446C>G , CM000671.2:g.127800446C>G GRCh38
NC_000009.11:g.130562725C>G , CM000671.1:g.130562725C>G GRCh37
NC_000009.10:g.129602546C>G NCBI36
NG_023245.1:g.2572C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3839C>G
ENST00000479375.6:n.132-3839C>G