Canonical Allele Identifier: CA126427

Gene: FGG

Linked Data

• ClinVar Variation Id: 16380
• ClinVar RCV Id: RCV000017802
• dbSNP Id: rs587776839
• MyVariant Identifiers: chr4:g.155530122T>A (hg19) ; chr4:g.154608970T>A (hg38)
• PubMed: PMID:1471077 ; PMID:17854317

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154608970T>A , CM000666.2:g.154608970T>A	GRCh38
NC_000004.11:g.155530122T>A , CM000666.1:g.155530122T>A	GRCh37
NC_000004.10:g.155749572T>A	NCBI36
NG_008834.1:g.8781A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.667-320A>T MANE Select	ENSP00000336829.3:n.667-320A>T
ENST00000336098.7:c.667-320A>T	ENSP00000336829.3:n.667-320A>T
ENST00000404648.7:c.667-320A>T	ENSP00000384860.3:n.667-320A>T
ENST00000405164.5:c.691-320A>T	ENSP00000384101.1:n.691-320A>T
ENST00000407946.5:c.691-320A>T	ENSP00000384552.1:n.691-320A>T
ENST00000443553.5:c.358-320A>T	ENSP00000407562.1:n.358-320A>T
ENST00000465913.1:n.215-320A>T
ENST00000492082.5:n.1209-320A>T
NM_000509.4:c.667-320A>T	NP_000500.2:n.667-320A>T
NM_000509.5:c.667-320A>T	NP_000500.2:n.667-320A>T
NM_021870.2:c.667-320A>T	NP_068656.2:n.667-320A>T
NM_021870.3:c.667-320A>T MANE Select	NP_068656.2:n.667-320A>T
NM_000509.6:c.667-320A>T	NP_000500.2:n.667-320A>T