Canonical Allele Identifier: CA446312346

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127693047G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357355G>T , CM000667.2:g.128357355G>T	GRCh38
NC_000005.9:g.127693047G>T , CM000667.1:g.127693047G>T	GRCh37
NC_000005.8:g.127720946G>T	NCBI36
NG_008750.1:g.185689C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2595C>A MANE Select	ENSP00000262464.4:p.Ala865=
ENST00000262464.8:c.2595C>A	ENSP00000262464.4:p.Ala865=
ENST00000508053.5:c.2595C>A	ENSP00000424571.1:p.Ala865=
ENST00000508989.5:c.2496C>A	ENSP00000425596.1:p.Ala832=
ENST00000619499.4:c.2592C>A	ENSP00000482132.1:p.Ala864=
NM_001999.3:c.2595C>A	NP_001990.2:p.Ala865=
XM_017009228.2:c.2442C>A	XP_016864717.1:p.Ala814=
NM_001999.4:c.2595C>A MANE Select	NP_001990.2:p.Ala865=