Canonical Allele Identifier: CA200280603
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs572436988

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800361A>G , CM000671.2:g.127800361A>G GRCh38
NC_000009.11:g.130562640A>G , CM000671.1:g.130562640A>G GRCh37
NC_000009.10:g.129602461A>G NCBI36
NG_023245.1:g.2487A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3924A>G
ENST00000479375.6:n.132-3924A>G