Canonical Allele Identifier: CA803637348

Gene: FBN2

Linked Data

• dbSNP Id: rs369591122
• gnomAD v3: 5-128335877-T-A
• gnomAD v4: 5-128335877-T-A
• MyVariant Identifiers: chr5:g.127671569T>A (hg19) ; chr5:g.128335877T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335877T>A , CM000667.2:g.128335877T>A	GRCh38
NC_000005.9:g.127671569T>A , CM000667.1:g.127671569T>A	GRCh37
NC_000005.8:g.127699468T>A	NCBI36
NG_008750.1:g.207167A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.508+111A>T
ENST00000703785.1:n.589+111A>T
ENST00000262464.9:c.3724+111A>T MANE Select	ENSP00000262464.4:n.3724+111A>T
ENST00000262464.8:c.3724+111A>T	ENSP00000262464.4:n.3724+111A>T
ENST00000507835.5:c.274+111A>T	ENSP00000426839.1:n.274+111A>T
ENST00000508053.5:c.3724+111A>T	ENSP00000424571.1:n.3724+111A>T
ENST00000508989.5:c.3625+111A>T	ENSP00000425596.1:n.3625+111A>T
ENST00000619499.4:c.3721+111A>T	ENSP00000482132.1:n.3721+111A>T
NM_001999.3:c.3724+111A>T	NP_001990.2:n.3724+111A>T
XM_017009228.2:c.3571+111A>T	XP_016864717.1:n.3571+111A>T
NM_001999.4:c.3724+111A>T MANE Select	NP_001990.2:n.3724+111A>T