Canonical Allele Identifier: CA3395133
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs568351052

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.609G>A
ENST00000703785.1:n.690G>A
ENST00000262464.9:c.3825G>A MANE Select ENSP00000262464.4:p.Met1275Ile
ENST00000262464.8:c.3825G>A ENSP00000262464.4:p.Met1275Ile
ENST00000507835.5:c.375G>A ENSP00000426839.1:p.Met125Ile
ENST00000508053.5:c.3825G>A ENSP00000424571.1:p.Met1275Ile
ENST00000508989.5:c.3726G>A ENSP00000425596.1:p.Met1242Ile
ENST00000619499.4:c.3822G>A ENSP00000482132.1:p.Met1274Ile
NM_001999.3:c.3825G>A NP_001990.2:p.Met1275Ile
XM_017009228.2:c.3672G>A XP_016864717.1:p.Met1224Ile
NM_001999.4:c.3825G>A MANE Select NP_001990.2:p.Met1275Ile