Canonical Allele Identifier: CA1581271169

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338949C= , CM000667.2:g.128338949C=	GRCh38
NC_000005.9:g.127674641C= , CM000667.1:g.127674641C=	GRCh37
NC_000005.8:g.127702540C=	NCBI36
NG_008750.1:g.204095G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001999.4:c.3456G= MANE Select	NP_001990.2:p.Met1152=
ENST00000262464.9:c.3456G= MANE Select	ENSP00000262464.4:p.Met1152=
NM_001999.3:c.3456G=	NP_001990.2:p.Met1152=
ENST00000262464.8:c.3456G=	ENSP00000262464.4:p.Met1152=
ENST00000507835.5:c.6G=	ENSP00000426839.1:p.Met2=
ENST00000508053.5:c.3456G=	ENSP00000424571.1:p.Met1152=
ENST00000508989.5:c.3357G=	ENSP00000425596.1:p.Met1119=
ENST00000619499.4:c.3453G=	ENSP00000482132.1:p.Met1151=
ENST00000703783.1:n.240G=
ENST00000703785.1:n.321G=
XM_017009228.2:c.3303G=	XP_016864717.1:p.Met1101=