Canonical Allele Identifier: CA2578395980
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128304864G>A , CM000667.2:g.128304864G>A GRCh38
NC_000005.9:g.127640556G>A , CM000667.1:g.127640556G>A GRCh37
NC_000005.8:g.127668455G>A NCBI36
NG_008750.1:g.238180C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.2584+93C>T
ENST00000703785.1:n.2503+93C>T
ENST00000262464.9:c.5800+93C>T MANE Select ENSP00000262464.4:n.5800+93C>T
ENST00000262464.8:c.5800+93C>T ENSP00000262464.4:n.5800+93C>T
ENST00000508053.5:c.5800+93C>T ENSP00000424571.1:n.5800+93C>T
ENST00000619499.4:c.5797+93C>T ENSP00000482132.1:n.5797+93C>T
NM_001999.3:c.5800+93C>T NP_001990.2:n.5800+93C>T
XM_017009228.2:c.5647+93C>T XP_016864717.1:n.5647+93C>T
NM_001999.4:c.5800+93C>T MANE Select NP_001990.2:n.5800+93C>T