Canonical Allele Identifier: CA1879991928
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800494C= , CM000671.2:g.127800494C= GRCh38
NC_000009.11:g.130562773C= , CM000671.1:g.130562773C= GRCh37
NC_000009.10:g.129602594C= NCBI36
NG_023245.1:g.2620C=

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3791C=
ENST00000479375.6:n.132-3791C=