Canonical Allele Identifier: CA108774424

Gene: FGG

Linked Data

• dbSNP Id: rs896318406
• gnomAD v3: 4-154605060-G-A
• gnomAD v4: 4-154605060-G-A
• MyVariant Identifiers: chr4:g.155526212G>A (hg19) ; chr4:g.154605060G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154605060G>A , CM000666.2:g.154605060G>A	GRCh38
NC_000004.11:g.155526212G>A , CM000666.1:g.155526212G>A	GRCh37
NC_000004.10:g.155745662G>A	NCBI36
NG_008834.1:g.12691C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1136C>T MANE Select	ENSP00000336829.3:p.Thr379Ile
ENST00000336098.7:c.1136C>T	ENSP00000336829.3:p.Thr379Ile
ENST00000404648.7:c.1136C>T	ENSP00000384860.3:p.Thr379Ile
ENST00000405164.5:c.1160C>T	ENSP00000384101.1:p.Thr387Ile
ENST00000407946.5:c.1160C>T	ENSP00000384552.1:p.Thr387Ile
ENST00000465913.1:n.684C>T
ENST00000492082.5:n.1678C>T
NM_000509.4:c.1136C>T	NP_000500.2:p.Thr379Ile
NM_000509.5:c.1136C>T	NP_000500.2:p.Thr379Ile
NM_021870.2:c.1136C>T	NP_068656.2:p.Thr379Ile
NM_021870.3:c.1136C>T MANE Select	NP_068656.2:p.Thr379Ile
NM_000509.6:c.1136C>T	NP_000500.2:p.Thr379Ile