Canonical Allele Identifier: CA2675117128
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335452T>C , CM000667.2:g.128335452T>C GRCh38
NC_000005.9:g.127671144T>C , CM000667.1:g.127671144T>C GRCh37
NC_000005.8:g.127699043T>C NCBI36
NG_008750.1:g.207592A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.631+3A>G
ENST00000703785.1:n.712+3A>G
ENST00000262464.9:c.3847+3A>G MANE Select ENSP00000262464.4:n.3847+3A>G
ENST00000262464.8:c.3847+3A>G ENSP00000262464.4:n.3847+3A>G
ENST00000507835.5:c.397+3A>G ENSP00000426839.1:n.397+3A>G
ENST00000508053.5:c.3847+3A>G ENSP00000424571.1:n.3847+3A>G
ENST00000508989.5:c.3748+3A>G ENSP00000425596.1:n.3748+3A>G
ENST00000619499.4:c.3844+3A>G ENSP00000482132.1:n.3844+3A>G
NM_001999.3:c.3847+3A>G NP_001990.2:n.3847+3A>G
XM_017009228.2:c.3694+3A>G XP_016864717.1:n.3694+3A>G
NM_001999.4:c.3847+3A>G MANE Select NP_001990.2:n.3847+3A>G