Canonical Allele Identifier: CA200299740
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814185C>G , CM000671.2:g.127814185C>G GRCh38
NC_000009.11:g.130576464C>G , CM000671.1:g.130576464C>G GRCh37
NC_000009.10:g.129616285C>G NCBI36
NG_009551.1:g.45584G>C , LRG_589:g.45584G>C
NG_023245.1:g.16311C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000467826.5:n.710-23C>G
XM_005251864.2:c.1484-23C>G XP_005251921.1:n.1484-23C>G
XM_005251864.4:c.1484-23C>G XP_005251921.1:n.1484-23C>G
XM_017014565.2:c.1334-23C>G XP_016870054.1:n.1334-23C>G
XR_242582.2:n.1381-23C>G
XR_242582.4:n.1379-23C>G