Canonical Allele Identifier: CA360767414
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357338C>T , CM000667.2:g.128357338C>T GRCh38
NC_000005.9:g.127693030C>T , CM000667.1:g.127693030C>T GRCh37
NC_000005.8:g.127720929C>T NCBI36
NG_008750.1:g.185706G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2612G>A MANE Select ENSP00000262464.4:p.Gly871Glu
ENST00000262464.8:c.2612G>A ENSP00000262464.4:p.Gly871Glu
ENST00000508053.5:c.2612G>A ENSP00000424571.1:p.Gly871Glu
ENST00000508989.5:c.2513G>A ENSP00000425596.1:p.Gly838Glu
ENST00000619499.4:c.2609G>A ENSP00000482132.1:p.Gly870Glu
NM_001999.3:c.2612G>A NP_001990.2:p.Gly871Glu
XM_017009228.2:c.2459G>A XP_016864717.1:p.Gly820Glu
NM_001999.4:c.2612G>A MANE Select NP_001990.2:p.Gly871Glu