Canonical Allele Identifier: CA360766162
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128300822C>T , CM000667.2:g.128300822C>T GRCh38
NC_000005.9:g.127636514C>T , CM000667.1:g.127636514C>T GRCh37
NC_000005.8:g.127664413C>T NCBI36
NG_008750.1:g.242222G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2945G>A
ENST00000703785.1:n.2864G>A
ENST00000262464.9:c.6161G>A MANE Select ENSP00000262464.4:p.Cys2054Tyr
ENST00000262464.8:c.6161G>A ENSP00000262464.4:p.Cys2054Tyr
ENST00000508053.5:c.6161G>A ENSP00000424571.1:p.Cys2054Tyr
ENST00000619499.4:c.6158G>A ENSP00000482132.1:p.Cys2053Tyr
NM_001999.3:c.6161G>A NP_001990.2:p.Cys2054Tyr
XM_017009228.2:c.6008G>A XP_016864717.1:p.Cys2003Tyr
NM_001999.4:c.6161G>A MANE Select NP_001990.2:p.Cys2054Tyr