Canonical Allele Identifier: CA2785995785
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800583G>T , CM000671.2:g.127800583G>T GRCh38
NC_000009.11:g.130562862G>T , CM000671.1:g.130562862G>T GRCh37
NC_000009.10:g.129602683G>T NCBI36
NG_023245.1:g.2709G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3702G>T
ENST00000479375.6:n.132-3702G>T