Canonical Allele Identifier: CA358535155

Gene: FGG

Linked Data

• dbSNP Id: rs1159291121
• gnomAD v2: 4-155526060-C-T
• gnomAD v4: 4-154604908-C-T
• MyVariant Identifiers: chr4:g.155526060C>T (hg19) ; chr4:g.154604908C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604908C>T , CM000666.2:g.154604908C>T	GRCh38
NC_000004.11:g.155526060C>T , CM000666.1:g.155526060C>T	GRCh37
NC_000004.10:g.155745510C>T	NCBI36
NG_008834.1:g.12843G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1288G>A MANE Select	ENSP00000336829.3:p.Gly430Arg
ENST00000336098.7:c.1288G>A	ENSP00000336829.3:p.Gly430Arg
ENST00000404648.7:c.1288G>A	ENSP00000384860.3:p.Gly430Arg
ENST00000405164.5:c.1312G>A	ENSP00000384101.1:p.Gly438Arg
ENST00000407946.5:c.1312G>A	ENSP00000384552.1:p.Gly438Arg
ENST00000465913.1:n.836G>A
ENST00000492082.5:n.1830G>A
NM_000509.4:c.1288G>A	NP_000500.2:p.Gly430Arg
NM_000509.5:c.1288G>A	NP_000500.2:p.Gly430Arg
NM_021870.2:c.1288G>A	NP_068656.2:p.Gly430Arg
NM_021870.3:c.1288G>A MANE Select	NP_068656.2:p.Gly430Arg
NM_000509.6:c.1288G>A	NP_000500.2:p.Gly430Arg