Canonical Allele Identifier: CA1879978302
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814187C= , CM000671.2:g.127814187C= GRCh38
NC_000009.11:g.130576466C= , CM000671.1:g.130576466C= GRCh37
NC_000009.10:g.129616287C= NCBI36
NG_009551.1:g.45582G= , LRG_589:g.45582G=
NG_023245.1:g.16313C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467826.5:n.710-21C=
XM_005251864.2:c.1484-21C= XP_005251921.1:n.1484-21C=
XM_005251864.4:c.1484-21C= XP_005251921.1:n.1484-21C=
XM_017014565.2:c.1334-21C= XP_016870054.1:n.1334-21C=
XR_242582.2:n.1381-21C=
XR_242582.4:n.1379-21C=