Canonical Allele Identifier: CA2785995772
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800489A>T , CM000671.2:g.127800489A>T GRCh38
NC_000009.11:g.130562768A>T , CM000671.1:g.130562768A>T GRCh37
NC_000009.10:g.129602589A>T NCBI36
NG_023245.1:g.2615A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3796A>T
ENST00000479375.6:n.132-3796A>T