Canonical Allele Identifier: CA1081366554

Gene: FBN2

Linked Data

• dbSNP Id: rs1751519805
• gnomAD v3: 5-128357083-C-CA
• gnomAD v4: 5-128357083-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357088dup , CM000667.2:g.128357088dup	GRCh38
NC_000005.9:g.127692780dup , CM000667.1:g.127692780dup	GRCh37
NC_000005.8:g.127720679dup	NCBI36
NG_008750.1:g.185960dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2674+192dup MANE Select	ENSP00000262464.4:n.2674+192dup
ENST00000262464.8:c.2674+192dup	ENSP00000262464.4:n.2674+192dup
ENST00000508053.5:c.2674+192dup	ENSP00000424571.1:n.2674+192dup
ENST00000508989.5:c.2575+192dup	ENSP00000425596.1:n.2575+192dup
ENST00000619499.4:c.2671+192dup	ENSP00000482132.1:n.2671+192dup
NM_001999.3:c.2674+192dup	NP_001990.2:n.2674+192dup
XM_017009228.2:c.2521+192dup	XP_016864717.1:n.2521+192dup
NM_001999.4:c.2674+192dup MANE Select	NP_001990.2:n.2674+192dup