Canonical Allele Identifier: CA860207761
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1465994815
MyVariant Identifiers: chr9:g.130562785G>A (hg19) chr9:g.127800506G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800506G>A , CM000671.2:g.127800506G>A GRCh38
NC_000009.11:g.130562785G>A , CM000671.1:g.130562785G>A GRCh37
NC_000009.10:g.129602606G>A NCBI36
NG_023245.1:g.2632G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3779G>A
ENST00000479375.6:n.132-3779G>A
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