Canonical Allele Identifier: CA1581253453
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128300821G= , CM000667.2:g.128300821G= GRCh38
NC_000005.9:g.127636513G= , CM000667.1:g.127636513G= GRCh37
NC_000005.8:g.127664412G= NCBI36
NG_008750.1:g.242223C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2946C=
ENST00000703785.1:n.2865C=
ENST00000262464.9:c.6162C= MANE Select ENSP00000262464.4:p.Cys2054=
ENST00000262464.8:c.6162C= ENSP00000262464.4:p.Cys2054=
ENST00000508053.5:c.6162C= ENSP00000424571.1:p.Cys2054=
ENST00000619499.4:c.6159C= ENSP00000482132.1:p.Cys2053=
NM_001999.3:c.6162C= NP_001990.2:p.Cys2054=
XM_017009228.2:c.6009C= XP_016864717.1:p.Cys2003=
NM_001999.4:c.6162C= MANE Select NP_001990.2:p.Cys2054=