Canonical Allele Identifier: CA360767531

Gene: FBN2

Linked Data

• gnomAD v4: 5-128357387-C-T
• MyVariant Identifiers: chr5:g.127693079C>T (hg19) ; chr5:g.128357387C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357387C>T , CM000667.2:g.128357387C>T	GRCh38
NC_000005.9:g.127693079C>T , CM000667.1:g.127693079C>T	GRCh37
NC_000005.8:g.127720978C>T	NCBI36
NG_008750.1:g.185657G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2563G>A MANE Select	ENSP00000262464.4:p.Glu855Lys
ENST00000262464.8:c.2563G>A	ENSP00000262464.4:p.Glu855Lys
ENST00000508053.5:c.2563G>A	ENSP00000424571.1:p.Glu855Lys
ENST00000508989.5:c.2464G>A	ENSP00000425596.1:p.Glu822Lys
ENST00000619499.4:c.2560G>A	ENSP00000482132.1:p.Glu854Lys
NM_001999.3:c.2563G>A	NP_001990.2:p.Glu855Lys
XM_017009228.2:c.2410G>A	XP_016864717.1:p.Glu804Lys
NM_001999.4:c.2563G>A MANE Select	NP_001990.2:p.Glu855Lys