Canonical Allele Identifier: CA446312362

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127693071T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357379T>C , CM000667.2:g.128357379T>C	GRCh38
NC_000005.9:g.127693071T>C , CM000667.1:g.127693071T>C	GRCh37
NC_000005.8:g.127720970T>C	NCBI36
NG_008750.1:g.185665A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2571A>G MANE Select	ENSP00000262464.4:p.Glu857=
ENST00000262464.8:c.2571A>G	ENSP00000262464.4:p.Glu857=
ENST00000508053.5:c.2571A>G	ENSP00000424571.1:p.Glu857=
ENST00000508989.5:c.2472A>G	ENSP00000425596.1:p.Glu824=
ENST00000619499.4:c.2568A>G	ENSP00000482132.1:p.Glu856=
NM_001999.3:c.2571A>G	NP_001990.2:p.Glu857=
XM_017009228.2:c.2418A>G	XP_016864717.1:p.Glu806=
NM_001999.4:c.2571A>G MANE Select	NP_001990.2:p.Glu857=