Canonical Allele Identifier: CA360767382
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128357325A>T , CM000667.2:g.128357325A>T GRCh38
NC_000005.9:g.127693017A>T , CM000667.1:g.127693017A>T GRCh37
NC_000005.8:g.127720916A>T NCBI36
NG_008750.1:g.185719T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.2625T>A MANE Select ENSP00000262464.4:p.Cys875Ter
ENST00000262464.8:c.2625T>A ENSP00000262464.4:p.Cys875Ter
ENST00000508053.5:c.2625T>A ENSP00000424571.1:p.Cys875Ter
ENST00000508989.5:c.2526T>A ENSP00000425596.1:p.Cys842Ter
ENST00000619499.4:c.2622T>A ENSP00000482132.1:p.Cys874Ter
NM_001999.3:c.2625T>A NP_001990.2:p.Cys875Ter
XM_017009228.2:c.2472T>A XP_016864717.1:p.Cys824Ter
NM_001999.4:c.2625T>A MANE Select NP_001990.2:p.Cys875Ter