Canonical Allele Identifier: CA360757473

Gene: FBN2

Linked Data

• ClinVar Variation Id: 1053570
• ClinVar RCV Id: RCV001361937
• dbSNP Id: rs755489065
• MyVariant Identifiers: chr5:g.127670946C>A (hg19) ; chr5:g.128335254C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335254C>A , CM000667.2:g.128335254C>A	GRCh38
NC_000005.9:g.127670946C>A , CM000667.1:g.127670946C>A	GRCh37
NC_000005.8:g.127698845C>A	NCBI36
NG_008750.1:g.207790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.673G>T
ENST00000703785.1:n.754G>T
ENST00000262464.9:c.3889G>T MANE Select	ENSP00000262464.4:p.Gly1297Cys
ENST00000262464.8:c.3889G>T	ENSP00000262464.4:p.Gly1297Cys
ENST00000507835.5:c.439G>T	ENSP00000426839.1:p.Gly147Cys
ENST00000508053.5:c.3889G>T	ENSP00000424571.1:p.Gly1297Cys
ENST00000508989.5:c.3790G>T	ENSP00000425596.1:p.Gly1264Cys
ENST00000619499.4:c.3886G>T	ENSP00000482132.1:p.Gly1296Cys
NM_001999.3:c.3889G>T	NP_001990.2:p.Gly1297Cys
XM_017009228.2:c.3736G>T	XP_016864717.1:p.Gly1246Cys
NM_001999.4:c.3889G>T MANE Select	NP_001990.2:p.Gly1297Cys