Canonical Allele Identifier: CA860207688
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1206267140
gnomAD v3: 9-127800335-A-G
gnomAD v4: 9-127800335-A-G
MyVariant Identifiers: chr9:g.130562614A>G (hg19) chr9:g.127800335A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800335A>G , CM000671.2:g.127800335A>G GRCh38
NC_000009.11:g.130562614A>G , CM000671.1:g.130562614A>G GRCh37
NC_000009.10:g.129602435A>G NCBI36
NG_023245.1:g.2461A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3950A>G
ENST00000479375.6:n.132-3950A>G
Search 100 bp 5'
Search 100 bp 3'