Canonical Allele Identifier: CA446310722

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127673795A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338103A>T , CM000667.2:g.128338103A>T	GRCh38
NC_000005.9:g.127673795A>T , CM000667.1:g.127673795A>T	GRCh37
NC_000005.8:g.127701694A>T	NCBI36
NG_008750.1:g.204941T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.276T>A
ENST00000703785.1:n.357T>A
ENST00000262464.9:c.3492T>A MANE Select	ENSP00000262464.4:p.Arg1164=
ENST00000262464.8:c.3492T>A	ENSP00000262464.4:p.Arg1164=
ENST00000507835.5:c.42T>A	ENSP00000426839.1:p.Arg14=
ENST00000508053.5:c.3492T>A	ENSP00000424571.1:p.Arg1164=
ENST00000508989.5:c.3393T>A	ENSP00000425596.1:p.Arg1131=
ENST00000619499.4:c.3489T>A	ENSP00000482132.1:p.Arg1163=
NM_001999.3:c.3492T>A	NP_001990.2:p.Arg1164=
XM_017009228.2:c.3339T>A	XP_016864717.1:p.Arg1113=
NM_001999.4:c.3492T>A MANE Select	NP_001990.2:p.Arg1164=