Canonical Allele Identifier: CA360755291
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128333002A>C , CM000667.2:g.128333002A>C GRCh38
NC_000005.9:g.127668694A>C , CM000667.1:g.127668694A>C GRCh37
NC_000005.8:g.127696593A>C NCBI36
NG_008750.1:g.210042T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.916T>G
ENST00000703785.1:n.997T>G
ENST00000262464.9:c.4132T>G MANE Select ENSP00000262464.4:p.Cys1378Gly
ENST00000262464.8:c.4132T>G ENSP00000262464.4:p.Cys1378Gly
ENST00000507835.5:c.682T>G ENSP00000426839.1:p.Cys228Gly
ENST00000508053.5:c.4132T>G ENSP00000424571.1:p.Cys1378Gly
ENST00000508989.5:c.4033T>G ENSP00000425596.1:p.Cys1345Gly
ENST00000619499.4:c.4129T>G ENSP00000482132.1:p.Cys1377Gly
NM_001999.3:c.4132T>G NP_001990.2:p.Cys1378Gly
XM_017009228.2:c.3979T>G XP_016864717.1:p.Cys1327Gly
NM_001999.4:c.4132T>G MANE Select NP_001990.2:p.Cys1378Gly