Canonical Allele Identifier: CA803645545

Gene: FBN2

Linked Data

• dbSNP Id: rs1310194532
• gnomAD v3: 5-128527396-A-T
• gnomAD v4: 5-128527396-A-T
• MyVariant Identifiers: chr5:g.127863089A>T (hg19) ; chr5:g.128527396A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128527396A>T , CM000667.2:g.128527396A>T	GRCh38
NC_000005.9:g.127863089A>T , CM000667.1:g.127863089A>T	GRCh37
NC_000005.8:g.127890988A>T	NCBI36
NG_008750.1:g.15647T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508053.6:c.532+476T>A	ENSP00000424571.2:n.532+476T>A
ENST00000703787.1:n.239+476T>A
ENST00000262464.9:c.532+476T>A MANE Select	ENSP00000262464.4:n.532+476T>A
ENST00000262464.8:c.532+476T>A	ENSP00000262464.4:n.532+476T>A
ENST00000502468.5:c.532+476T>A	ENSP00000424753.1:n.532+476T>A
ENST00000508053.5:c.532+476T>A	ENSP00000424571.1:n.532+476T>A
ENST00000508989.5:c.433+476T>A	ENSP00000425596.1:n.433+476T>A
ENST00000514742.1:n.1152+476T>A
ENST00000619499.4:c.532+476T>A	ENSP00000482132.1:n.532+476T>A
ENST00000620257.1:c.532+476T>A	ENSP00000479157.1:n.532+476T>A
NM_001999.3:c.532+476T>A	NP_001990.2:n.532+476T>A
XM_017009228.2:c.532+476T>A	XP_016864717.1:n.532+476T>A
NM_001999.4:c.532+476T>A MANE Select	NP_001990.2:n.532+476T>A