Canonical Allele Identifier: CA590597112
Gene: FPGS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800534A>T , CM000671.2:g.127800534A>T GRCh38
NC_000009.11:g.130562813A>T , CM000671.1:g.130562813A>T GRCh37
NC_000009.10:g.129602634A>T NCBI36
NG_023245.1:g.2660A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3751A>T
ENST00000479375.6:n.132-3751A>T