Canonical Allele Identifier: CA1581273730
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128344391A= , CM000667.2:g.128344391A= GRCh38
NC_000005.9:g.127680083A= , CM000667.1:g.127680083A= GRCh37
NC_000005.8:g.127707982A= NCBI36
NG_008750.1:g.198653T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.3337T= MANE Select ENSP00000262464.4:p.Cys1113=
ENST00000262464.8:c.3337T= ENSP00000262464.4:p.Cys1113=
ENST00000508053.5:c.3337T= ENSP00000424571.1:p.Cys1113=
ENST00000508989.5:c.3238T= ENSP00000425596.1:p.Cys1080=
ENST00000619499.4:c.3334T= ENSP00000482132.1:p.Cys1112=
NM_001999.3:c.3337T= NP_001990.2:p.Cys1113=
XM_017009228.2:c.3184T= XP_016864717.1:p.Cys1062=
NM_001999.4:c.3337T= MANE Select NP_001990.2:p.Cys1113=