Canonical Allele Identifier: CA1879991794
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1588543897

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800435A>C , CM000671.2:g.127800435A>C GRCh38
NC_000009.11:g.130562714A>C , CM000671.1:g.130562714A>C GRCh37
NC_000009.10:g.129602535A>C NCBI36
NG_023245.1:g.2561A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3850A>C
ENST00000479375.6:n.132-3850A>C