Canonical Allele Identifier: CA1581270717

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338003A= , CM000667.2:g.128338003A=	GRCh38
NC_000005.9:g.127673695A= , CM000667.1:g.127673695A=	GRCh37
NC_000005.8:g.127701594A=	NCBI36
NG_008750.1:g.205041T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.376T=
ENST00000703785.1:n.457T=
ENST00000262464.9:c.3592T= MANE Select	ENSP00000262464.4:p.Cys1198=
ENST00000262464.8:c.3592T=	ENSP00000262464.4:p.Cys1198=
ENST00000507835.5:c.142T=	ENSP00000426839.1:p.Cys48=
ENST00000508053.5:c.3592T=	ENSP00000424571.1:p.Cys1198=
ENST00000508989.5:c.3493T=	ENSP00000425596.1:p.Cys1165=
ENST00000619499.4:c.3589T=	ENSP00000482132.1:p.Cys1197=
NM_001999.3:c.3592T=	NP_001990.2:p.Cys1198=
XM_017009228.2:c.3439T=	XP_016864717.1:p.Cys1147=
NM_001999.4:c.3592T= MANE Select	NP_001990.2:p.Cys1198=