Canonical Allele Identifier: CA360758173

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127671271T>A (hg19) ; chr5:g.128335579T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335579T>A , CM000667.2:g.128335579T>A	GRCh38
NC_000005.9:g.127671271T>A , CM000667.1:g.127671271T>A	GRCh37
NC_000005.8:g.127699170T>A	NCBI36
NG_008750.1:g.207465A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.509-2A>T
ENST00000703785.1:n.590-2A>T
ENST00000262464.9:c.3725-2A>T MANE Select	ENSP00000262464.4:n.3725-2A>T
ENST00000262464.8:c.3725-2A>T	ENSP00000262464.4:n.3725-2A>T
ENST00000507835.5:c.275-2A>T	ENSP00000426839.1:n.275-2A>T
ENST00000508053.5:c.3725-2A>T	ENSP00000424571.1:n.3725-2A>T
ENST00000508989.5:c.3626-2A>T	ENSP00000425596.1:n.3626-2A>T
ENST00000619499.4:c.3722-2A>T	ENSP00000482132.1:n.3722-2A>T
NM_001999.3:c.3725-2A>T	NP_001990.2:n.3725-2A>T
XM_017009228.2:c.3572-2A>T	XP_016864717.1:n.3572-2A>T
NM_001999.4:c.3725-2A>T MANE Select	NP_001990.2:n.3725-2A>T