Canonical Allele Identifier: CA860207715
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1174646134

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800425C>T , CM000671.2:g.127800425C>T GRCh38
NC_000009.11:g.130562704C>T , CM000671.1:g.130562704C>T GRCh37
NC_000009.10:g.129602525C>T NCBI36
NG_023245.1:g.2551C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3860C>T
ENST00000479375.6:n.132-3860C>T