Canonical Allele Identifier: CA360757882

Gene: FBN2

Linked Data

• ClinVar Variation Id: 984565
• ClinVar RCV Id: RCV001264655
• dbSNP Id: rs1750805468
• MyVariant Identifiers: chr5:g.127670988C>T (hg19) ; chr5:g.128335296C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335296C>T , CM000667.2:g.128335296C>T	GRCh38
NC_000005.9:g.127670988C>T , CM000667.1:g.127670988C>T	GRCh37
NC_000005.8:g.127698887C>T	NCBI36
NG_008750.1:g.207748G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.632-1G>A
ENST00000703785.1:n.713-1G>A
ENST00000262464.9:c.3848-1G>A MANE Select	ENSP00000262464.4:n.3848-1G>A
ENST00000262464.8:c.3848-1G>A	ENSP00000262464.4:n.3848-1G>A
ENST00000507835.5:c.398-1G>A	ENSP00000426839.1:n.398-1G>A
ENST00000508053.5:c.3848-1G>A	ENSP00000424571.1:n.3848-1G>A
ENST00000508989.5:c.3749-1G>A	ENSP00000425596.1:n.3749-1G>A
ENST00000619499.4:c.3845-1G>A	ENSP00000482132.1:n.3845-1G>A
NM_001999.3:c.3848-1G>A	NP_001990.2:n.3848-1G>A
XM_017009228.2:c.3695-1G>A	XP_016864717.1:n.3695-1G>A
NM_001999.4:c.3848-1G>A MANE Select	NP_001990.2:n.3848-1G>A