Canonical Allele Identifier: CA126983115

Gene: FBN2

Linked Data

• dbSNP Id: rs867477517
• MyVariant Identifiers: chr5:g.127640688T>A (hg19) ; chr5:g.128304996T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128304996T>A , CM000667.2:g.128304996T>A	GRCh38
NC_000005.9:g.127640688T>A , CM000667.1:g.127640688T>A	GRCh37
NC_000005.8:g.127668587T>A	NCBI36
NG_008750.1:g.238048A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.2545A>T
ENST00000703785.1:n.2464A>T
ENST00000262464.9:c.5761A>T MANE Select	ENSP00000262464.4:p.Asn1921Tyr
ENST00000262464.8:c.5761A>T	ENSP00000262464.4:p.Asn1921Tyr
ENST00000508053.5:c.5761A>T	ENSP00000424571.1:p.Asn1921Tyr
ENST00000619499.4:c.5758A>T	ENSP00000482132.1:p.Asn1920Tyr
NM_001999.3:c.5761A>T	NP_001990.2:p.Asn1921Tyr
XM_017009228.2:c.5608A>T	XP_016864717.1:p.Asn1870Tyr
NM_001999.4:c.5761A>T MANE Select	NP_001990.2:p.Asn1921Tyr