Canonical Allele Identifier: CA1504952224

Gene: FGG

Linked Data

• dbSNP Id: rs1049636

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604818G>C , CM000666.2:g.154604818G>C	GRCh38
NC_000004.11:g.155525970G>C , CM000666.1:g.155525970G>C	GRCh37
NC_000004.10:g.155745420G>C	NCBI36
NG_008834.1:g.12933C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336098.8:c.*16C>G MANE Select	ENSP00000336829.3:n.*16C>G
ENST00000336098.7:c.*16C>G	ENSP00000336829.3:n.*16C>G
ENST00000404648.7:c.1299+79C>G	ENSP00000384860.3:n.1299+79C>G
ENST00000405164.5:c.1323+79C>G	ENSP00000384101.1:n.1323+79C>G
ENST00000407946.5:c.*16C>G	ENSP00000384552.1:n.*16C>G
ENST00000465913.1:n.926C>G
ENST00000492082.5:n.1841+79C>G
NM_000509.4:c.1299+79C>G	NP_000500.2:n.1299+79C>G
NM_000509.5:c.1299+79C>G	NP_000500.2:n.1299+79C>G
NM_021870.2:c.*16C>G	NP_068656.2:n.*16C>G
NM_021870.3:c.*16C>G MANE Select	NP_068656.2:n.*16C>G
NM_000509.6:c.1299+79C>G	NP_000500.2:n.1299+79C>G