Canonical Allele Identifier: CA200299751
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814197G>A , CM000671.2:g.127814197G>A GRCh38
NC_000009.11:g.130576476G>A , CM000671.1:g.130576476G>A GRCh37
NC_000009.10:g.129616297G>A NCBI36
NG_009551.1:g.45572C>T , LRG_589:g.45572C>T
NG_023245.1:g.16323G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000467826.5:n.710-11G>A
XM_005251864.2:c.1484-11G>A XP_005251921.1:n.1484-11G>A
XM_005251864.4:c.1484-11G>A XP_005251921.1:n.1484-11G>A
XM_017014565.2:c.1334-11G>A XP_016870054.1:n.1334-11G>A
XR_242582.2:n.1381-11G>A
XR_242582.4:n.1379-11G>A