Canonical Allele Identifier: CA2691804525
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814183G>T , CM000671.2:g.127814183G>T GRCh38
NC_000009.11:g.130576462G>T , CM000671.1:g.130576462G>T GRCh37
NC_000009.10:g.129616283G>T NCBI36
NG_009551.1:g.45586C>A , LRG_589:g.45586C>A
NG_023245.1:g.16309G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000467826.5:n.710-25G>T
XM_005251864.2:c.1484-25G>T XP_005251921.1:n.1484-25G>T
XM_005251864.4:c.1484-25G>T XP_005251921.1:n.1484-25G>T
XM_017014565.2:c.1334-25G>T XP_016870054.1:n.1334-25G>T
XR_242582.2:n.1381-25G>T
XR_242582.4:n.1379-25G>T