Canonical Allele Identifier: CA446312302
Gene: FBN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.127692975G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357283G>T , CM000667.2:g.128357283G>T GRCh38
NC_000005.9:g.127692975G>T , CM000667.1:g.127692975G>T GRCh37
NC_000005.8:g.127720874G>T NCBI36
NG_008750.1:g.185761C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262464.9:c.2667C>A MANE Select ENSP00000262464.4:p.Ile889=
ENST00000262464.8:c.2667C>A ENSP00000262464.4:p.Ile889=
ENST00000508053.5:c.2667C>A ENSP00000424571.1:p.Ile889=
ENST00000508989.5:c.2568C>A ENSP00000425596.1:p.Ile856=
ENST00000619499.4:c.2664C>A ENSP00000482132.1:p.Ile888=
NM_001999.3:c.2667C>A NP_001990.2:p.Ile889=
XM_017009228.2:c.2514C>A XP_016864717.1:p.Ile838=
NM_001999.4:c.2667C>A MANE Select NP_001990.2:p.Ile889=