Canonical Allele Identifier: CA127015661

Gene: FBN2

Linked Data

• dbSNP Id: rs933902577
• MyVariant Identifiers: chr5:g.127674871T>A (hg19) ; chr5:g.128339179T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128339179T>A , CM000667.2:g.128339179T>A	GRCh38
NC_000005.9:g.127674871T>A , CM000667.1:g.127674871T>A	GRCh37
NC_000005.8:g.127702770T>A	NCBI36
NG_008750.1:g.203865A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.10A>T
ENST00000703785.1:n.91A>T
ENST00000262464.9:c.3344-118A>T MANE Select	ENSP00000262464.4:n.3344-118A>T
ENST00000262464.8:c.3344-118A>T	ENSP00000262464.4:n.3344-118A>T
ENST00000507835.5:c.-225A>T	ENSP00000426839.1:n.-225A>T
ENST00000508053.5:c.3344-118A>T	ENSP00000424571.1:n.3344-118A>T
ENST00000508989.5:c.3245-118A>T	ENSP00000425596.1:n.3245-118A>T
ENST00000619499.4:c.3341-118A>T	ENSP00000482132.1:n.3341-118A>T
NM_001999.3:c.3344-118A>T	NP_001990.2:n.3344-118A>T
XM_017009228.2:c.3191-118A>T	XP_016864717.1:n.3191-118A>T
NM_001999.4:c.3344-118A>T MANE Select	NP_001990.2:n.3344-118A>T