Canonical Allele Identifier: CA360767297

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127692982C>T (hg19) ; chr5:g.128357290C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357290C>T , CM000667.2:g.128357290C>T	GRCh38
NC_000005.9:g.127692982C>T , CM000667.1:g.127692982C>T	GRCh37
NC_000005.8:g.127720881C>T	NCBI36
NG_008750.1:g.185754G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2660G>A MANE Select	ENSP00000262464.4:p.Gly887Glu
ENST00000262464.8:c.2660G>A	ENSP00000262464.4:p.Gly887Glu
ENST00000508053.5:c.2660G>A	ENSP00000424571.1:p.Gly887Glu
ENST00000508989.5:c.2561G>A	ENSP00000425596.1:p.Gly854Glu
ENST00000619499.4:c.2657G>A	ENSP00000482132.1:p.Gly886Glu
NM_001999.3:c.2660G>A	NP_001990.2:p.Gly887Glu
XM_017009228.2:c.2507G>A	XP_016864717.1:p.Gly836Glu
NM_001999.4:c.2660G>A MANE Select	NP_001990.2:p.Gly887Glu