Canonical Allele Identifier: CA360754591
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128332916A>C , CM000667.2:g.128332916A>C GRCh38
NC_000005.9:g.127668608A>C , CM000667.1:g.127668608A>C GRCh37
NC_000005.8:g.127696507A>C NCBI36
NG_008750.1:g.210128T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.1002T>G
ENST00000703785.1:n.1083T>G
ENST00000262464.9:c.4218T>G MANE Select ENSP00000262464.4:p.Cys1406Trp
ENST00000262464.8:c.4218T>G ENSP00000262464.4:p.Cys1406Trp
ENST00000507835.5:c.768T>G ENSP00000426839.1:p.Cys256Trp
ENST00000508053.5:c.4218T>G ENSP00000424571.1:p.Cys1406Trp
ENST00000508989.5:c.4119T>G ENSP00000425596.1:p.Cys1373Trp
ENST00000619499.4:c.4215T>G ENSP00000482132.1:p.Cys1405Trp
NM_001999.3:c.4218T>G NP_001990.2:p.Cys1406Trp
XM_017009228.2:c.4065T>G XP_016864717.1:p.Cys1355Trp
NM_001999.4:c.4218T>G MANE Select NP_001990.2:p.Cys1406Trp