Canonical Allele Identifier: CA446305689

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127597545T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128261853T>G , CM000667.2:g.128261853T>G	GRCh38
NC_000005.9:g.127597545T>G , CM000667.1:g.127597545T>G	GRCh37
NC_000005.8:g.127625444T>G	NCBI36
NG_008750.1:g.281191A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.8247A>C MANE Select	ENSP00000262464.4:p.Thr2749=
ENST00000262464.8:c.8247A>C	ENSP00000262464.4:p.Thr2749=
ENST00000508053.5:c.8247A>C	ENSP00000424571.1:p.Thr2749=
ENST00000619499.4:c.8244A>C	ENSP00000482132.1:p.Thr2748=
NM_001999.3:c.8247A>C	NP_001990.2:p.Thr2749=
XM_017009228.2:c.8094A>C	XP_016864717.1:p.Thr2698=
NM_001999.4:c.8247A>C MANE Select	NP_001990.2:p.Thr2749=