Canonical Allele Identifier: CA1879991714
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829550935

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800385C>T , CM000671.2:g.127800385C>T GRCh38
NC_000009.11:g.130562664C>T , CM000671.1:g.130562664C>T GRCh37
NC_000009.10:g.129602485C>T NCBI36
NG_023245.1:g.2511C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3900C>T
ENST00000479375.6:n.132-3900C>T