Canonical Allele Identifier: CA446306353

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127640668C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128304976C>T , CM000667.2:g.128304976C>T	GRCh38
NC_000005.9:g.127640668C>T , CM000667.1:g.127640668C>T	GRCh37
NC_000005.8:g.127668567C>T	NCBI36
NG_008750.1:g.238068G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.2565G>A
ENST00000703785.1:n.2484G>A
ENST00000262464.9:c.5781G>A MANE Select	ENSP00000262464.4:p.Gln1927=
ENST00000262464.8:c.5781G>A	ENSP00000262464.4:p.Gln1927=
ENST00000508053.5:c.5781G>A	ENSP00000424571.1:p.Gln1927=
ENST00000619499.4:c.5778G>A	ENSP00000482132.1:p.Gln1926=
NM_001999.3:c.5781G>A	NP_001990.2:p.Gln1927=
XM_017009228.2:c.5628G>A	XP_016864717.1:p.Gln1876=
NM_001999.4:c.5781G>A MANE Select	NP_001990.2:p.Gln1927=