Canonical Allele Identifier: CA1581269599
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335474T= , CM000667.2:g.128335474T= GRCh38
NC_000005.9:g.127671166T= , CM000667.1:g.127671166T= GRCh37
NC_000005.8:g.127699065T= NCBI36
NG_008750.1:g.207570A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.612A=
ENST00000703785.1:n.693A=
ENST00000262464.9:c.3828A= MANE Select ENSP00000262464.4:p.Pro1276=
ENST00000262464.8:c.3828A= ENSP00000262464.4:p.Pro1276=
ENST00000507835.5:c.378A= ENSP00000426839.1:p.Pro126=
ENST00000508053.5:c.3828A= ENSP00000424571.1:p.Pro1276=
ENST00000508989.5:c.3729A= ENSP00000425596.1:p.Pro1243=
ENST00000619499.4:c.3825A= ENSP00000482132.1:p.Pro1275=
NM_001999.3:c.3828A= NP_001990.2:p.Pro1276=
XM_017009228.2:c.3675A= XP_016864717.1:p.Pro1225=
NM_001999.4:c.3828A= MANE Select NP_001990.2:p.Pro1276=