Canonical Allele Identifier: CA1581269600
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335477C= , CM000667.2:g.128335477C= GRCh38
NC_000005.9:g.127671169C= , CM000667.1:g.127671169C= GRCh37
NC_000005.8:g.127699068C= NCBI36
NG_008750.1:g.207567G=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.609G=
ENST00000703785.1:n.690G=
ENST00000262464.9:c.3825G= MANE Select ENSP00000262464.4:p.Met1275=
ENST00000262464.8:c.3825G= ENSP00000262464.4:p.Met1275=
ENST00000507835.5:c.375G= ENSP00000426839.1:p.Met125=
ENST00000508053.5:c.3825G= ENSP00000424571.1:p.Met1275=
ENST00000508989.5:c.3726G= ENSP00000425596.1:p.Met1242=
ENST00000619499.4:c.3822G= ENSP00000482132.1:p.Met1274=
NM_001999.3:c.3825G= NP_001990.2:p.Met1275=
XM_017009228.2:c.3672G= XP_016864717.1:p.Met1224=
NM_001999.4:c.3825G= MANE Select NP_001990.2:p.Met1275=