Canonical Allele Identifier: CA446309536

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668701A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128333009A>C , CM000667.2:g.128333009A>C	GRCh38
NC_000005.9:g.127668701A>C , CM000667.1:g.127668701A>C	GRCh37
NC_000005.8:g.127696600A>C	NCBI36
NG_008750.1:g.210035T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.909T>G
ENST00000703785.1:n.990T>G
ENST00000262464.9:c.4125T>G MANE Select	ENSP00000262464.4:p.Ala1375=
ENST00000262464.8:c.4125T>G	ENSP00000262464.4:p.Ala1375=
ENST00000507835.5:c.675T>G	ENSP00000426839.1:p.Ala225=
ENST00000508053.5:c.4125T>G	ENSP00000424571.1:p.Ala1375=
ENST00000508989.5:c.4026T>G	ENSP00000425596.1:p.Ala1342=
ENST00000619499.4:c.4122T>G	ENSP00000482132.1:p.Ala1374=
NM_001999.3:c.4125T>G	NP_001990.2:p.Ala1375=
XM_017009228.2:c.3972T>G	XP_016864717.1:p.Ala1324=
NM_001999.4:c.4125T>G MANE Select	NP_001990.2:p.Ala1375=