Canonical Allele Identifier: CA2675118105
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128344310T>A , CM000667.2:g.128344310T>A GRCh38
NC_000005.9:g.127680002T>A , CM000667.1:g.127680002T>A GRCh37
NC_000005.8:g.127707901T>A NCBI36
NG_008750.1:g.198734A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262464.9:c.3343+75A>T MANE Select ENSP00000262464.4:n.3343+75A>T
ENST00000262464.8:c.3343+75A>T ENSP00000262464.4:n.3343+75A>T
ENST00000508053.5:c.3343+75A>T ENSP00000424571.1:n.3343+75A>T
ENST00000508989.5:c.3244+75A>T ENSP00000425596.1:n.3244+75A>T
ENST00000619499.4:c.3340+75A>T ENSP00000482132.1:n.3340+75A>T
NM_001999.3:c.3343+75A>T NP_001990.2:n.3343+75A>T
XM_017009228.2:c.3190+75A>T XP_016864717.1:n.3190+75A>T
NM_001999.4:c.3343+75A>T MANE Select NP_001990.2:n.3343+75A>T