Canonical Allele Identifier: CA2578444127

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335951G>A , CM000667.2:g.128335951G>A	GRCh38
NC_000005.9:g.127671643G>A , CM000667.1:g.127671643G>A	GRCh37
NC_000005.8:g.127699542G>A	NCBI36
NG_008750.1:g.207093C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.508+37C>T
ENST00000703785.1:n.589+37C>T
ENST00000262464.9:c.3724+37C>T MANE Select	ENSP00000262464.4:n.3724+37C>T
ENST00000262464.8:c.3724+37C>T	ENSP00000262464.4:n.3724+37C>T
ENST00000507835.5:c.274+37C>T	ENSP00000426839.1:n.274+37C>T
ENST00000508053.5:c.3724+37C>T	ENSP00000424571.1:n.3724+37C>T
ENST00000508989.5:c.3625+37C>T	ENSP00000425596.1:n.3625+37C>T
ENST00000619499.4:c.3721+37C>T	ENSP00000482132.1:n.3721+37C>T
NM_001999.3:c.3724+37C>T	NP_001990.2:n.3724+37C>T
XM_017009228.2:c.3571+37C>T	XP_016864717.1:n.3571+37C>T
NM_001999.4:c.3724+37C>T MANE Select	NP_001990.2:n.3724+37C>T