Canonical Allele Identifier: CA13000813
Gene: FPGS HGNC NCBI

Linked Data

dbSNP Id: rs1544105

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800446C>T , CM000671.2:g.127800446C>T GRCh38
NC_000009.11:g.130562725C>T , CM000671.1:g.130562725C>T GRCh37
NC_000009.10:g.129602546C>T NCBI36
NG_023245.1:g.2572C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000479147.6:n.217-3839C>T
ENST00000479375.6:n.132-3839C>T