Canonical Allele Identifier: CA360755502

Gene: FBN2

Linked Data

• gnomAD v4: 5-128333029-C-T
• MyVariant Identifiers: chr5:g.127668721C>T (hg19) ; chr5:g.128333029C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128333029C>T , CM000667.2:g.128333029C>T	GRCh38
NC_000005.9:g.127668721C>T , CM000667.1:g.127668721C>T	GRCh37
NC_000005.8:g.127696620C>T	NCBI36
NG_008750.1:g.210015G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.889G>A
ENST00000703785.1:n.970G>A
ENST00000262464.9:c.4105G>A MANE Select	ENSP00000262464.4:p.Asp1369Asn
ENST00000262464.8:c.4105G>A	ENSP00000262464.4:p.Asp1369Asn
ENST00000507835.5:c.655G>A	ENSP00000426839.1:p.Asp219Asn
ENST00000508053.5:c.4105G>A	ENSP00000424571.1:p.Asp1369Asn
ENST00000508989.5:c.4006G>A	ENSP00000425596.1:p.Asp1336Asn
ENST00000619499.4:c.4102G>A	ENSP00000482132.1:p.Asp1368Asn
NM_001999.3:c.4105G>A	NP_001990.2:p.Asp1369Asn
XM_017009228.2:c.3952G>A	XP_016864717.1:p.Asp1318Asn
NM_001999.4:c.4105G>A MANE Select	NP_001990.2:p.Asp1369Asn