Canonical Allele Identifier: CA1581268443

Gene: FBN2

Linked Data

• dbSNP Id: rs764661746

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128333081T>A , CM000667.2:g.128333081T>A	GRCh38
NC_000005.9:g.127668773T>A , CM000667.1:g.127668773T>A	GRCh37
NC_000005.8:g.127696672T>A	NCBI36
NG_008750.1:g.209963A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.884-47A>T
ENST00000703785.1:n.965-47A>T
ENST00000262464.9:c.4100-47A>T MANE Select	ENSP00000262464.4:n.4100-47A>T
ENST00000262464.8:c.4100-47A>T	ENSP00000262464.4:n.4100-47A>T
ENST00000507835.5:c.650-47A>T	ENSP00000426839.1:n.650-47A>T
ENST00000508053.5:c.4100-47A>T	ENSP00000424571.1:n.4100-47A>T
ENST00000508989.5:c.4001-47A>T	ENSP00000425596.1:n.4001-47A>T
ENST00000619499.4:c.4097-47A>T	ENSP00000482132.1:n.4097-47A>T
NM_001999.3:c.4100-47A>T	NP_001990.2:n.4100-47A>T
XM_017009228.2:c.3947-47A>T	XP_016864717.1:n.3947-47A>T
NM_001999.4:c.4100-47A>T MANE Select	NP_001990.2:n.4100-47A>T