Canonical Allele Identifier: CA360766146
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128300819A>G , CM000667.2:g.128300819A>G GRCh38
NC_000005.9:g.127636511A>G , CM000667.1:g.127636511A>G GRCh37
NC_000005.8:g.127664410A>G NCBI36
NG_008750.1:g.242225T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2948T>C
ENST00000703785.1:n.2867T>C
ENST00000262464.9:c.6164T>C MANE Select ENSP00000262464.4:p.Ile2055Thr
ENST00000262464.8:c.6164T>C ENSP00000262464.4:p.Ile2055Thr
ENST00000508053.5:c.6164T>C ENSP00000424571.1:p.Ile2055Thr
ENST00000619499.4:c.6161T>C ENSP00000482132.1:p.Ile2054Thr
NM_001999.3:c.6164T>C NP_001990.2:p.Ile2055Thr
XM_017009228.2:c.6011T>C XP_016864717.1:p.Ile2004Thr
NM_001999.4:c.6164T>C MANE Select NP_001990.2:p.Ile2055Thr