Canonical Allele Identifier: CA360755273
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128333000G>C , CM000667.2:g.128333000G>C GRCh38
NC_000005.9:g.127668692G>C , CM000667.1:g.127668692G>C GRCh37
NC_000005.8:g.127696591G>C NCBI36
NG_008750.1:g.210044C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.918C>G
ENST00000703785.1:n.999C>G
ENST00000262464.9:c.4134C>G MANE Select ENSP00000262464.4:p.Cys1378Trp
ENST00000262464.8:c.4134C>G ENSP00000262464.4:p.Cys1378Trp
ENST00000507835.5:c.684C>G ENSP00000426839.1:p.Cys228Trp
ENST00000508053.5:c.4134C>G ENSP00000424571.1:p.Cys1378Trp
ENST00000508989.5:c.4035C>G ENSP00000425596.1:p.Cys1345Trp
ENST00000619499.4:c.4131C>G ENSP00000482132.1:p.Cys1377Trp
NM_001999.3:c.4134C>G NP_001990.2:p.Cys1378Trp
XM_017009228.2:c.3981C>G XP_016864717.1:p.Cys1327Trp
NM_001999.4:c.4134C>G MANE Select NP_001990.2:p.Cys1378Trp