Canonical Allele Identifier: CA1504952149
Gene: FGG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604647C= , CM000666.2:g.154604647C= GRCh38
NC_000004.11:g.155525799C= , CM000666.1:g.155525799C= GRCh37
NC_000004.10:g.155745249C= NCBI36
NG_008834.1:g.13104G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336098.8:c.*187G= MANE Select ENSP00000336829.3:n.*187G=
ENST00000336098.7:c.*187G= ENSP00000336829.3:n.*187G=
ENST00000404648.7:c.1299+250G= ENSP00000384860.3:n.1299+250G=
ENST00000405164.5:c.1323+250G= ENSP00000384101.1:n.1323+250G=
ENST00000407946.5:c.*187G= ENSP00000384552.1:n.*187G=
ENST00000465913.1:n.1097G=
ENST00000492082.5:n.1841+250G=
NM_000509.4:c.1299+250G= NP_000500.2:n.1299+250G=
NM_000509.5:c.1299+250G= NP_000500.2:n.1299+250G=
NM_021870.2:c.*187G= NP_068656.2:n.*187G=
NM_021870.3:c.*187G= MANE Select NP_068656.2:n.*187G=
NM_000509.6:c.1299+250G= NP_000500.2:n.1299+250G=