Canonical Allele Identifier: CA360761646
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128344389G>T , CM000667.2:g.128344389G>T GRCh38
NC_000005.9:g.127680081G>T , CM000667.1:g.127680081G>T GRCh37
NC_000005.8:g.127707980G>T NCBI36
NG_008750.1:g.198655C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.3339C>A MANE Select ENSP00000262464.4:p.Cys1113Ter
ENST00000262464.8:c.3339C>A ENSP00000262464.4:p.Cys1113Ter
ENST00000508053.5:c.3339C>A ENSP00000424571.1:p.Cys1113Ter
ENST00000508989.5:c.3240C>A ENSP00000425596.1:p.Cys1080Ter
ENST00000619499.4:c.3336C>A ENSP00000482132.1:p.Cys1112Ter
NM_001999.3:c.3339C>A NP_001990.2:p.Cys1113Ter
XM_017009228.2:c.3186C>A XP_016864717.1:p.Cys1062Ter
NM_001999.4:c.3339C>A MANE Select NP_001990.2:p.Cys1113Ter