Canonical Allele Identifier: CA1581255421

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128305058G= , CM000667.2:g.128305058G=	GRCh38
NC_000005.9:g.127640750G= , CM000667.1:g.127640750G=	GRCh37
NC_000005.8:g.127668649G=	NCBI36
NG_008750.1:g.237986C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.2483C=
ENST00000703785.1:n.2402C=
ENST00000262464.9:c.5699C= MANE Select	ENSP00000262464.4:p.Pro1900=
ENST00000262464.8:c.5699C=	ENSP00000262464.4:p.Pro1900=
ENST00000508053.5:c.5699C=	ENSP00000424571.1:p.Pro1900=
ENST00000619499.4:c.5696C=	ENSP00000482132.1:p.Pro1899=
NM_001999.3:c.5699C=	NP_001990.2:p.Pro1900=
XM_017009228.2:c.5546C=	XP_016864717.1:p.Pro1849=
NM_001999.4:c.5699C= MANE Select	NP_001990.2:p.Pro1900=