Canonical Allele Identifier: CA360759952

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127674685A>T (hg19) ; chr5:g.128338993A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338993A>T , CM000667.2:g.128338993A>T	GRCh38
NC_000005.9:g.127674685A>T , CM000667.1:g.127674685A>T	GRCh37
NC_000005.8:g.127702584A>T	NCBI36
NG_008750.1:g.204051T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.196T>A
ENST00000703785.1:n.277T>A
ENST00000262464.9:c.3412T>A MANE Select	ENSP00000262464.4:p.Phe1138Ile
ENST00000262464.8:c.3412T>A	ENSP00000262464.4:p.Phe1138Ile
ENST00000507835.5:c.-39T>A	ENSP00000426839.1:n.-39T>A
ENST00000508053.5:c.3412T>A	ENSP00000424571.1:p.Phe1138Ile
ENST00000508989.5:c.3313T>A	ENSP00000425596.1:p.Phe1105Ile
ENST00000619499.4:c.3409T>A	ENSP00000482132.1:p.Phe1137Ile
NM_001999.3:c.3412T>A	NP_001990.2:p.Phe1138Ile
XM_017009228.2:c.3259T>A	XP_016864717.1:p.Phe1087Ile
NM_001999.4:c.3412T>A MANE Select	NP_001990.2:p.Phe1138Ile