Canonical Allele Identifier: CA1581282262

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357309T= , CM000667.2:g.128357309T=	GRCh38
NC_000005.9:g.127693001T= , CM000667.1:g.127693001T=	GRCh37
NC_000005.8:g.127720900T=	NCBI36
NG_008750.1:g.185735A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2641A= MANE Select	ENSP00000262464.4:p.Ser881=
ENST00000262464.8:c.2641A=	ENSP00000262464.4:p.Ser881=
ENST00000508053.5:c.2641A=	ENSP00000424571.1:p.Ser881=
ENST00000508989.5:c.2542A=	ENSP00000425596.1:p.Ser848=
ENST00000619499.4:c.2638A=	ENSP00000482132.1:p.Ser880=
NM_001999.3:c.2641A=	NP_001990.2:p.Ser881=
XM_017009228.2:c.2488A=	XP_016864717.1:p.Ser830=
NM_001999.4:c.2641A= MANE Select	NP_001990.2:p.Ser881=