Canonical Allele Identifier: CA3115469
Gene: FGG HGNC NCBI

Linked Data

dbSNP Id: rs758920678

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604937A>G , CM000666.2:g.154604937A>G GRCh38
NC_000004.11:g.155526089A>G , CM000666.1:g.155526089A>G GRCh37
NC_000004.10:g.155745539A>G NCBI36
NG_008834.1:g.12814T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336098.8:c.1259T>C MANE Select ENSP00000336829.3:p.Ile420Thr
ENST00000336098.7:c.1259T>C ENSP00000336829.3:p.Ile420Thr
ENST00000404648.7:c.1259T>C ENSP00000384860.3:p.Ile420Thr
ENST00000405164.5:c.1283T>C ENSP00000384101.1:p.Ile428Thr
ENST00000407946.5:c.1283T>C ENSP00000384552.1:p.Ile428Thr
ENST00000465913.1:n.807T>C
ENST00000492082.5:n.1801T>C
NM_000509.4:c.1259T>C NP_000500.2:p.Ile420Thr
NM_000509.5:c.1259T>C NP_000500.2:p.Ile420Thr
NM_021870.2:c.1259T>C NP_068656.2:p.Ile420Thr
NM_021870.3:c.1259T>C MANE Select NP_068656.2:p.Ile420Thr
NM_000509.6:c.1259T>C NP_000500.2:p.Ile420Thr