Canonical Allele Identifier: CA360767389
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357327A>T , CM000667.2:g.128357327A>T GRCh38
NC_000005.9:g.127693019A>T , CM000667.1:g.127693019A>T GRCh37
NC_000005.8:g.127720918A>T NCBI36
NG_008750.1:g.185717T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2623T>A MANE Select ENSP00000262464.4:p.Cys875Ser
ENST00000262464.8:c.2623T>A ENSP00000262464.4:p.Cys875Ser
ENST00000508053.5:c.2623T>A ENSP00000424571.1:p.Cys875Ser
ENST00000508989.5:c.2524T>A ENSP00000425596.1:p.Cys842Ser
ENST00000619499.4:c.2620T>A ENSP00000482132.1:p.Cys874Ser
NM_001999.3:c.2623T>A NP_001990.2:p.Cys875Ser
XM_017009228.2:c.2470T>A XP_016864717.1:p.Cys824Ser
NM_001999.4:c.2623T>A MANE Select NP_001990.2:p.Cys875Ser