Canonical Allele Identifier: CA360750662
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128395187C>A , CM000667.2:g.128395187C>A GRCh38
NC_000005.9:g.127730880C>A , CM000667.1:g.127730880C>A GRCh37
NC_000005.8:g.127758779C>A NCBI36
NG_008750.1:g.147856G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703787.1:n.873G>T
ENST00000262464.9:c.1166G>T MANE Select ENSP00000262464.4:p.Cys389Phe
ENST00000262464.8:c.1166G>T ENSP00000262464.4:p.Cys389Phe
ENST00000508053.5:c.1166G>T ENSP00000424571.1:p.Cys389Phe
ENST00000508989.5:c.1067G>T ENSP00000425596.1:p.Cys356Phe
ENST00000619499.4:c.1163G>T ENSP00000482132.1:p.Cys388Phe
NM_001999.3:c.1166G>T NP_001990.2:p.Cys389Phe
XM_017009228.2:c.1079-1819G>T XP_016864717.1:n.1079-1819G>T
NM_001999.4:c.1166G>T MANE Select NP_001990.2:p.Cys389Phe