Canonical Allele Identifier: CA360750697
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128395191A>C , CM000667.2:g.128395191A>C GRCh38
NC_000005.9:g.127730884A>C , CM000667.1:g.127730884A>C GRCh37
NC_000005.8:g.127758783A>C NCBI36
NG_008750.1:g.147852T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703787.1:n.869T>G
ENST00000262464.9:c.1162T>G MANE Select ENSP00000262464.4:p.Cys388Gly
ENST00000262464.8:c.1162T>G ENSP00000262464.4:p.Cys388Gly
ENST00000508053.5:c.1162T>G ENSP00000424571.1:p.Cys388Gly
ENST00000508989.5:c.1063T>G ENSP00000425596.1:p.Cys355Gly
ENST00000619499.4:c.1159T>G ENSP00000482132.1:p.Cys387Gly
NM_001999.3:c.1162T>G NP_001990.2:p.Cys388Gly
XM_017009228.2:c.1079-1823T>G XP_016864717.1:n.1079-1823T>G
NM_001999.4:c.1162T>G MANE Select NP_001990.2:p.Cys388Gly