Canonical Allele Identifier: CA3173348428
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814188T= , CM000671.2:g.127814188T= GRCh38
NC_000009.11:g.130576467T= , CM000671.1:g.130576467T= GRCh37
NC_000009.10:g.129616288T= NCBI36
NG_009551.1:g.45581A= , LRG_589:g.45581A=
NG_023245.1:g.16314T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467826.5:n.710-20T=
XM_005251864.2:c.1484-20T= XP_005251921.1:n.1484-20T=
XM_005251864.4:c.1484-20T= XP_005251921.1:n.1484-20T=
XM_017014565.2:c.1334-20T= XP_016870054.1:n.1334-20T=
XR_242582.2:n.1381-20T=
XR_242582.4:n.1379-20T=