Canonical Allele Identifier: CA1504952180
Gene: FGG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604724T= , CM000666.2:g.154604724T= GRCh38
NC_000004.11:g.155525876T= , CM000666.1:g.155525876T= GRCh37
NC_000004.10:g.155745326T= NCBI36
NG_008834.1:g.13027A=

Transcript Alleles

HGVS Amino-acid change
ENST00000336098.8:c.*110A= MANE Select ENSP00000336829.3:n.*110A=
ENST00000336098.7:c.*110A= ENSP00000336829.3:n.*110A=
ENST00000404648.7:c.1299+173A= ENSP00000384860.3:n.1299+173A=
ENST00000405164.5:c.1323+173A= ENSP00000384101.1:n.1323+173A=
ENST00000407946.5:c.*110A= ENSP00000384552.1:n.*110A=
ENST00000465913.1:n.1020A=
ENST00000492082.5:n.1841+173A=
NM_000509.4:c.1299+173A= NP_000500.2:n.1299+173A=
NM_000509.5:c.1299+173A= NP_000500.2:n.1299+173A=
NM_021870.2:c.*110A= NP_068656.2:n.*110A=
NM_021870.3:c.*110A= MANE Select NP_068656.2:n.*110A=
NM_000509.6:c.1299+173A= NP_000500.2:n.1299+173A=