Canonical Allele Identifier: CA360758136
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335565C>A , CM000667.2:g.128335565C>A GRCh38
NC_000005.9:g.127671257C>A , CM000667.1:g.127671257C>A GRCh37
NC_000005.8:g.127699156C>A NCBI36
NG_008750.1:g.207479G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.521G>T
ENST00000703785.1:n.602G>T
ENST00000262464.9:c.3737G>T MANE Select ENSP00000262464.4:p.Cys1246Phe
ENST00000262464.8:c.3737G>T ENSP00000262464.4:p.Cys1246Phe
ENST00000507835.5:c.287G>T ENSP00000426839.1:p.Cys96Phe
ENST00000508053.5:c.3737G>T ENSP00000424571.1:p.Cys1246Phe
ENST00000508989.5:c.3638G>T ENSP00000425596.1:p.Cys1213Phe
ENST00000619499.4:c.3734G>T ENSP00000482132.1:p.Cys1245Phe
NM_001999.3:c.3737G>T NP_001990.2:p.Cys1246Phe
XM_017009228.2:c.3584G>T XP_016864717.1:p.Cys1195Phe
NM_001999.4:c.3737G>T MANE Select NP_001990.2:p.Cys1246Phe