Canonical Allele Identifier: CA360767298

Gene: FBN2

Linked Data

• dbSNP Id: rs1321557283
• gnomAD v2: 5-127692983-C-T
• gnomAD v4: 5-128357291-C-T
• MyVariant Identifiers: chr5:g.127692983C>T (hg19) ; chr5:g.128357291C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357291C>T , CM000667.2:g.128357291C>T	GRCh38
NC_000005.9:g.127692983C>T , CM000667.1:g.127692983C>T	GRCh37
NC_000005.8:g.127720882C>T	NCBI36
NG_008750.1:g.185753G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2659G>A MANE Select	ENSP00000262464.4:p.Gly887Arg
ENST00000262464.8:c.2659G>A	ENSP00000262464.4:p.Gly887Arg
ENST00000508053.5:c.2659G>A	ENSP00000424571.1:p.Gly887Arg
ENST00000508989.5:c.2560G>A	ENSP00000425596.1:p.Gly854Arg
ENST00000619499.4:c.2656G>A	ENSP00000482132.1:p.Gly886Arg
NM_001999.3:c.2659G>A	NP_001990.2:p.Gly887Arg
XM_017009228.2:c.2506G>A	XP_016864717.1:p.Gly836Arg
NM_001999.4:c.2659G>A MANE Select	NP_001990.2:p.Gly887Arg