Canonical Allele Identifier: CA360754841

Gene: FBN2

Linked Data

• ClinVar Variation Id: 1509864
• ClinVar RCV Id: RCV002011348
• dbSNP Id: rs886038935
• MyVariant Identifiers: chr5:g.127668642C>T (hg19) ; chr5:g.128332950C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332950C>T , CM000667.2:g.128332950C>T	GRCh38
NC_000005.9:g.127668642C>T , CM000667.1:g.127668642C>T	GRCh37
NC_000005.8:g.127696541C>T	NCBI36
NG_008750.1:g.210094G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.968G>A
ENST00000703785.1:n.1049G>A
ENST00000262464.9:c.4184G>A MANE Select	ENSP00000262464.4:p.Cys1395Tyr
ENST00000262464.8:c.4184G>A	ENSP00000262464.4:p.Cys1395Tyr
ENST00000507835.5:c.734G>A	ENSP00000426839.1:p.Cys245Tyr
ENST00000508053.5:c.4184G>A	ENSP00000424571.1:p.Cys1395Tyr
ENST00000508989.5:c.4085G>A	ENSP00000425596.1:p.Cys1362Tyr
ENST00000619499.4:c.4181G>A	ENSP00000482132.1:p.Cys1394Tyr
NM_001999.3:c.4184G>A	NP_001990.2:p.Cys1395Tyr
XM_017009228.2:c.4031G>A	XP_016864717.1:p.Cys1344Tyr
NM_001999.4:c.4184G>A MANE Select	NP_001990.2:p.Cys1395Tyr