Canonical Allele Identifier: CA1581269553
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335368T= , CM000667.2:g.128335368T= GRCh38
NC_000005.9:g.127671060T= , CM000667.1:g.127671060T= GRCh37
NC_000005.8:g.127698959T= NCBI36
NG_008750.1:g.207676A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.632-73A=
ENST00000703785.1:n.713-73A=
ENST00000262464.9:c.3848-73A= MANE Select ENSP00000262464.4:n.3848-73A=
ENST00000262464.8:c.3848-73A= ENSP00000262464.4:n.3848-73A=
ENST00000507835.5:c.398-73A= ENSP00000426839.1:n.398-73A=
ENST00000508053.5:c.3848-73A= ENSP00000424571.1:n.3848-73A=
ENST00000508989.5:c.3749-73A= ENSP00000425596.1:n.3749-73A=
ENST00000619499.4:c.3845-73A= ENSP00000482132.1:n.3845-73A=
NM_001999.3:c.3848-73A= NP_001990.2:n.3848-73A=
XM_017009228.2:c.3695-73A= XP_016864717.1:n.3695-73A=
NM_001999.4:c.3848-73A= MANE Select NP_001990.2:n.3848-73A=