Canonical Allele Identifier: CA1581255381
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128304960T= , CM000667.2:g.128304960T= GRCh38
NC_000005.9:g.127640652T= , CM000667.1:g.127640652T= GRCh37
NC_000005.8:g.127668551T= NCBI36
NG_008750.1:g.238084A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2581A=
ENST00000703785.1:n.2500A=
ENST00000262464.9:c.5797A= MANE Select ENSP00000262464.4:p.Met1933=
ENST00000262464.8:c.5797A= ENSP00000262464.4:p.Met1933=
ENST00000508053.5:c.5797A= ENSP00000424571.1:p.Met1933=
ENST00000619499.4:c.5794A= ENSP00000482132.1:p.Met1932=
NM_001999.3:c.5797A= NP_001990.2:p.Met1933=
XM_017009228.2:c.5644A= XP_016864717.1:p.Met1882=
NM_001999.4:c.5797A= MANE Select NP_001990.2:p.Met1933=