Canonical Allele Identifier: CA3115562

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154608608A>G , CM000666.2:g.154608608A>G	GRCh38
NC_000004.11:g.155529760A>G , CM000666.1:g.155529760A>G	GRCh37
NC_000004.10:g.155749210A>G	NCBI36
NG_008834.1:g.9143T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021870.3:c.709T>C MANE Select	NP_068656.2:p.Tyr237His
ENST00000336098.8:c.709T>C MANE Select	ENSP00000336829.3:p.Tyr237His
NM_000509.4:c.709T>C	NP_000500.2:p.Tyr237His
NM_000509.5:c.709T>C	NP_000500.2:p.Tyr237His
NM_000509.6:c.709T>C	NP_000500.2:p.Tyr237His
NM_021870.2:c.709T>C	NP_068656.2:p.Tyr237His
ENST00000336098.7:c.709T>C	ENSP00000336829.3:p.Tyr237His
ENST00000404648.7:c.709T>C	ENSP00000384860.3:p.Tyr237His
ENST00000405164.5:c.733T>C	ENSP00000384101.1:p.Tyr245His
ENST00000407946.5:c.733T>C	ENSP00000384552.1:p.Tyr245His
ENST00000465913.1:n.257T>C
ENST00000492082.5:n.1251T>C