Canonical Allele Identifier: CA915943207

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154609607A>T , CM000666.2:g.154609607A>T	GRCh38
NC_000004.11:g.155530759A>T , CM000666.1:g.155530759A>T	GRCh37
NC_000004.10:g.155750209A>T	NCBI36
NG_008834.1:g.8144T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021870.3:c.666+23T>A MANE Select	NP_068656.2:n.666+23T>A
ENST00000336098.8:c.666+23T>A MANE Select	ENSP00000336829.3:n.666+23T>A
NM_000509.4:c.666+23T>A	NP_000500.2:n.666+23T>A
NM_000509.5:c.666+23T>A	NP_000500.2:n.666+23T>A
NM_000509.6:c.666+23T>A	NP_000500.2:n.666+23T>A
NM_021870.2:c.666+23T>A	NP_068656.2:n.666+23T>A
ENST00000336098.7:c.666+23T>A	ENSP00000336829.3:n.666+23T>A
ENST00000404648.7:c.666+23T>A	ENSP00000384860.3:n.666+23T>A
ENST00000405164.5:c.690+23T>A	ENSP00000384101.1:n.690+23T>A
ENST00000407946.5:c.690+23T>A	ENSP00000384552.1:n.690+23T>A
ENST00000443553.5:c.357+23T>A	ENSP00000407562.1:n.357+23T>A
ENST00000465913.1:n.214+23T>A
ENST00000492082.5:n.1208+23T>A