Canonical Allele Identifier: CA360739716
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128304963A>T , CM000667.2:g.128304963A>T GRCh38
NC_000005.9:g.127640655A>T , CM000667.1:g.127640655A>T GRCh37
NC_000005.8:g.127668554A>T NCBI36
NG_008750.1:g.238081T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2578T>A
ENST00000703785.1:n.2497T>A
ENST00000262464.9:c.5794T>A MANE Select ENSP00000262464.4:p.Cys1932Ser
ENST00000262464.8:c.5794T>A ENSP00000262464.4:p.Cys1932Ser
ENST00000508053.5:c.5794T>A ENSP00000424571.1:p.Cys1932Ser
ENST00000619499.4:c.5791T>A ENSP00000482132.1:p.Cys1931Ser
NM_001999.3:c.5794T>A NP_001990.2:p.Cys1932Ser
XM_017009228.2:c.5641T>A XP_016864717.1:p.Cys1881Ser
NM_001999.4:c.5794T>A MANE Select NP_001990.2:p.Cys1932Ser