Canonical Allele Identifier: CA3115474

Gene: FGG

Linked Data

• dbSNP Id: rs754193577
• ExAC: 4:155526118 C / T
• gnomAD v2: 4-155526118-C-T
• gnomAD v3: 4-154604966-C-T
• gnomAD v4: 4-154604966-C-T
• COSMIC: COSM1695131
• MyVariant Identifiers: chr4:g.155526118C>T (hg19) ; chr4:g.154604966C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604966C>T , CM000666.2:g.154604966C>T	GRCh38
NC_000004.11:g.155526118C>T , CM000666.1:g.155526118C>T	GRCh37
NC_000004.10:g.155745568C>T	NCBI36
NG_008834.1:g.12785G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1230G>A MANE Select	ENSP00000336829.3:p.Met410Ile
ENST00000336098.7:c.1230G>A	ENSP00000336829.3:p.Met410Ile
ENST00000404648.7:c.1230G>A	ENSP00000384860.3:p.Met410Ile
ENST00000405164.5:c.1254G>A	ENSP00000384101.1:p.Met418Ile
ENST00000407946.5:c.1254G>A	ENSP00000384552.1:p.Met418Ile
ENST00000465913.1:n.778G>A
ENST00000492082.5:n.1772G>A
NM_000509.4:c.1230G>A	NP_000500.2:p.Met410Ile
NM_000509.5:c.1230G>A	NP_000500.2:p.Met410Ile
NM_021870.2:c.1230G>A	NP_068656.2:p.Met410Ile
NM_021870.3:c.1230G>A MANE Select	NP_068656.2:p.Met410Ile
NM_000509.6:c.1230G>A	NP_000500.2:p.Met410Ile