Canonical Allele Identifier: CA446308395

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127863584A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128527891A>T , CM000667.2:g.128527891A>T	GRCh38
NC_000005.9:g.127863584A>T , CM000667.1:g.127863584A>T	GRCh37
NC_000005.8:g.127891483A>T	NCBI36
NG_008750.1:g.15152T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508053.6:c.513T>A	ENSP00000424571.2:p.Ile171=
ENST00000703787.1:n.220T>A
ENST00000262464.9:c.513T>A MANE Select	ENSP00000262464.4:p.Ile171=
ENST00000262464.8:c.513T>A	ENSP00000262464.4:p.Ile171=
ENST00000502468.5:c.513T>A	ENSP00000424753.1:p.Ile171=
ENST00000508053.5:c.513T>A	ENSP00000424571.1:p.Ile171=
ENST00000508989.5:c.414T>A	ENSP00000425596.1:p.Ile138=
ENST00000514742.1:n.1133T>A
ENST00000619499.4:c.513T>A	ENSP00000482132.1:p.Ile171=
ENST00000620257.1:c.513T>A	ENSP00000479157.1:p.Ile171=
NM_001999.3:c.513T>A	NP_001990.2:p.Ile171=
XM_017009228.2:c.513T>A	XP_016864717.1:p.Ile171=
NM_001999.4:c.513T>A MANE Select	NP_001990.2:p.Ile171=