Canonical Allele Identifier: CA1581269597
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335467T= , CM000667.2:g.128335467T= GRCh38
NC_000005.9:g.127671159T= , CM000667.1:g.127671159T= GRCh37
NC_000005.8:g.127699058T= NCBI36
NG_008750.1:g.207577A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.619A=
ENST00000703785.1:n.700A=
ENST00000262464.9:c.3835A= MANE Select ENSP00000262464.4:p.Arg1279=
ENST00000262464.8:c.3835A= ENSP00000262464.4:p.Arg1279=
ENST00000507835.5:c.385A= ENSP00000426839.1:p.Arg129=
ENST00000508053.5:c.3835A= ENSP00000424571.1:p.Arg1279=
ENST00000508989.5:c.3736A= ENSP00000425596.1:p.Arg1246=
ENST00000619499.4:c.3832A= ENSP00000482132.1:p.Arg1278=
NM_001999.3:c.3835A= NP_001990.2:p.Arg1279=
XM_017009228.2:c.3682A= XP_016864717.1:p.Arg1228=
NM_001999.4:c.3835A= MANE Select NP_001990.2:p.Arg1279=