Canonical Allele Identifier: CA360757935
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335475G>A , CM000667.2:g.128335475G>A GRCh38
NC_000005.9:g.127671167G>A , CM000667.1:g.127671167G>A GRCh37
NC_000005.8:g.127699066G>A NCBI36
NG_008750.1:g.207569C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.611C>T
ENST00000703785.1:n.692C>T
ENST00000262464.9:c.3827C>T MANE Select ENSP00000262464.4:p.Pro1276Leu
ENST00000262464.8:c.3827C>T ENSP00000262464.4:p.Pro1276Leu
ENST00000507835.5:c.377C>T ENSP00000426839.1:p.Pro126Leu
ENST00000508053.5:c.3827C>T ENSP00000424571.1:p.Pro1276Leu
ENST00000508989.5:c.3728C>T ENSP00000425596.1:p.Pro1243Leu
ENST00000619499.4:c.3824C>T ENSP00000482132.1:p.Pro1275Leu
NM_001999.3:c.3827C>T NP_001990.2:p.Pro1276Leu
XM_017009228.2:c.3674C>T XP_016864717.1:p.Pro1225Leu
NM_001999.4:c.3827C>T MANE Select NP_001990.2:p.Pro1276Leu