Canonical Allele Identifier: CA360755461

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668717T>C (hg19) ; chr5:g.128333025T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128333025T>C , CM000667.2:g.128333025T>C	GRCh38
NC_000005.9:g.127668717T>C , CM000667.1:g.127668717T>C	GRCh37
NC_000005.8:g.127696616T>C	NCBI36
NG_008750.1:g.210019A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.893A>G
ENST00000703785.1:n.974A>G
ENST00000262464.9:c.4109A>G MANE Select	ENSP00000262464.4:p.Glu1370Gly
ENST00000262464.8:c.4109A>G	ENSP00000262464.4:p.Glu1370Gly
ENST00000507835.5:c.659A>G	ENSP00000426839.1:p.Glu220Gly
ENST00000508053.5:c.4109A>G	ENSP00000424571.1:p.Glu1370Gly
ENST00000508989.5:c.4010A>G	ENSP00000425596.1:p.Glu1337Gly
ENST00000619499.4:c.4106A>G	ENSP00000482132.1:p.Glu1369Gly
NM_001999.3:c.4109A>G	NP_001990.2:p.Glu1370Gly
XM_017009228.2:c.3956A>G	XP_016864717.1:p.Glu1319Gly
NM_001999.4:c.4109A>G MANE Select	NP_001990.2:p.Glu1370Gly