Canonical Allele Identifier: CA360754207

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127666379C>A (hg19) ; chr5:g.128330687C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330687C>A , CM000667.2:g.128330687C>A	GRCh38
NC_000005.9:g.127666379C>A , CM000667.1:g.127666379C>A	GRCh37
NC_000005.8:g.127694278C>A	NCBI36
NG_008750.1:g.212357G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.1015G>T
ENST00000703785.1:n.1096G>T
ENST00000262464.9:c.4231G>T MANE Select	ENSP00000262464.4:p.Glu1411Ter
ENST00000262464.8:c.4231G>T	ENSP00000262464.4:p.Glu1411Ter
ENST00000507835.5:c.781G>T	ENSP00000426839.1:p.Glu261Ter
ENST00000508053.5:c.4231G>T	ENSP00000424571.1:p.Glu1411Ter
ENST00000508989.5:c.4132G>T	ENSP00000425596.1:p.Glu1378Ter
ENST00000619499.4:c.4228G>T	ENSP00000482132.1:p.Glu1410Ter
NM_001999.3:c.4231G>T	NP_001990.2:p.Glu1411Ter
XM_017009228.2:c.4078G>T	XP_016864717.1:p.Glu1360Ter
NM_001999.4:c.4231G>T MANE Select	NP_001990.2:p.Glu1411Ter