Canonical Allele Identifier: CA360757945
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335479T>C , CM000667.2:g.128335479T>C GRCh38
NC_000005.9:g.127671171T>C , CM000667.1:g.127671171T>C GRCh37
NC_000005.8:g.127699070T>C NCBI36
NG_008750.1:g.207565A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.607A>G
ENST00000703785.1:n.688A>G
ENST00000262464.9:c.3823A>G MANE Select ENSP00000262464.4:p.Met1275Val
ENST00000262464.8:c.3823A>G ENSP00000262464.4:p.Met1275Val
ENST00000507835.5:c.373A>G ENSP00000426839.1:p.Met125Val
ENST00000508053.5:c.3823A>G ENSP00000424571.1:p.Met1275Val
ENST00000508989.5:c.3724A>G ENSP00000425596.1:p.Met1242Val
ENST00000619499.4:c.3820A>G ENSP00000482132.1:p.Met1274Val
NM_001999.3:c.3823A>G NP_001990.2:p.Met1275Val
XM_017009228.2:c.3670A>G XP_016864717.1:p.Met1224Val
NM_001999.4:c.3823A>G MANE Select NP_001990.2:p.Met1275Val