Canonical Allele Identifier: CA360758129
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335562A>C , CM000667.2:g.128335562A>C GRCh38
NC_000005.9:g.127671254A>C , CM000667.1:g.127671254A>C GRCh37
NC_000005.8:g.127699153A>C NCBI36
NG_008750.1:g.207482T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.524T>G
ENST00000703785.1:n.605T>G
ENST00000262464.9:c.3740T>G MANE Select ENSP00000262464.4:p.Met1247Arg
ENST00000262464.8:c.3740T>G ENSP00000262464.4:p.Met1247Arg
ENST00000507835.5:c.290T>G ENSP00000426839.1:p.Met97Arg
ENST00000508053.5:c.3740T>G ENSP00000424571.1:p.Met1247Arg
ENST00000508989.5:c.3641T>G ENSP00000425596.1:p.Met1214Arg
ENST00000619499.4:c.3737T>G ENSP00000482132.1:p.Met1246Arg
NM_001999.3:c.3740T>G NP_001990.2:p.Met1247Arg
XM_017009228.2:c.3587T>G XP_016864717.1:p.Met1196Arg
NM_001999.4:c.3740T>G MANE Select NP_001990.2:p.Met1247Arg