Canonical Allele Identifier: CA1879991656
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1829550236

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800331A>C , CM000671.2:g.127800331A>C GRCh38
NC_000009.11:g.130562610A>C , CM000671.1:g.130562610A>C GRCh37
NC_000009.10:g.129602431A>C NCBI36
NG_023245.1:g.2457A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3954A>C
ENST00000479375.6:n.132-3954A>C