Canonical Allele Identifier: CA446309429

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668617G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332925G>T , CM000667.2:g.128332925G>T	GRCh38
NC_000005.9:g.127668617G>T , CM000667.1:g.127668617G>T	GRCh37
NC_000005.8:g.127696516G>T	NCBI36
NG_008750.1:g.210119C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.993C>A
ENST00000703785.1:n.1074C>A
ENST00000262464.9:c.4209C>A MANE Select	ENSP00000262464.4:p.Gly1403=
ENST00000262464.8:c.4209C>A	ENSP00000262464.4:p.Gly1403=
ENST00000507835.5:c.759C>A	ENSP00000426839.1:p.Gly253=
ENST00000508053.5:c.4209C>A	ENSP00000424571.1:p.Gly1403=
ENST00000508989.5:c.4110C>A	ENSP00000425596.1:p.Gly1370=
ENST00000619499.4:c.4206C>A	ENSP00000482132.1:p.Gly1402=
NM_001999.3:c.4209C>A	NP_001990.2:p.Gly1403=
XM_017009228.2:c.4056C>A	XP_016864717.1:p.Gly1352=
NM_001999.4:c.4209C>A MANE Select	NP_001990.2:p.Gly1403=