Canonical Allele Identifier: CA11664959

Gene: FGG

Linked Data

• ClinVar Variation Id: 1234766
• ClinVar RCV Id: RCV001621530
• dbSNP Id: rs2066861
• gnomAD v2: 4-155527436-C-T
• gnomAD v3: 4-154606284-C-T
• gnomAD v4: 4-154606284-C-T
• MyVariant Identifiers: chr4:g.155527436C>T (hg19) ; chr4:g.154606284C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154606284C>T , CM000666.2:g.154606284C>T	GRCh38
NC_000004.11:g.155527436C>T , CM000666.1:g.155527436C>T	GRCh37
NC_000004.10:g.155746886C>T	NCBI36
NG_008834.1:g.11467G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336098.8:c.1129+421G>A MANE Select	ENSP00000336829.3:n.1129+421G>A
ENST00000336098.7:c.1129+421G>A	ENSP00000336829.3:n.1129+421G>A
ENST00000404648.7:c.1129+421G>A	ENSP00000384860.3:n.1129+421G>A
ENST00000405164.5:c.1153+421G>A	ENSP00000384101.1:n.1153+421G>A
ENST00000407946.5:c.1153+421G>A	ENSP00000384552.1:n.1153+421G>A
ENST00000465913.1:n.677+421G>A
ENST00000492082.5:n.1671+421G>A
NM_000509.4:c.1129+421G>A	NP_000500.2:n.1129+421G>A
NM_000509.5:c.1129+421G>A	NP_000500.2:n.1129+421G>A
NM_021870.2:c.1129+421G>A	NP_068656.2:n.1129+421G>A
NM_021870.3:c.1129+421G>A MANE Select	NP_068656.2:n.1129+421G>A
NM_000509.6:c.1129+421G>A	NP_000500.2:n.1129+421G>A