Canonical Allele Identifier: CA446309195

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127666299G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330607G>T , CM000667.2:g.128330607G>T	GRCh38
NC_000005.9:g.127666299G>T , CM000667.1:g.127666299G>T	GRCh37
NC_000005.8:g.127694198G>T	NCBI36
NG_008750.1:g.212437C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.1095C>A
ENST00000703785.1:n.1176C>A
ENST00000262464.9:c.4311C>A MANE Select	ENSP00000262464.4:p.Ser1437=
ENST00000262464.8:c.4311C>A	ENSP00000262464.4:p.Ser1437=
ENST00000507835.5:c.861C>A	ENSP00000426839.1:p.Ser287=
ENST00000508053.5:c.4311C>A	ENSP00000424571.1:p.Ser1437=
ENST00000508989.5:c.4212C>A	ENSP00000425596.1:p.Ser1404=
ENST00000619499.4:c.4308C>A	ENSP00000482132.1:p.Ser1436=
NM_001999.3:c.4311C>A	NP_001990.2:p.Ser1437=
XM_017009228.2:c.4158C>A	XP_016864717.1:p.Ser1386=
NM_001999.4:c.4311C>A MANE Select	NP_001990.2:p.Ser1437=