Canonical Allele Identifier: CA446306110
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs1296023744

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128395174G>A , CM000667.2:g.128395174G>A GRCh38
NC_000005.9:g.127730867G>A , CM000667.1:g.127730867G>A GRCh37
NC_000005.8:g.127758766G>A NCBI36
NG_008750.1:g.147869C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703787.1:n.886C>T
ENST00000262464.9:c.1179C>T MANE Select ENSP00000262464.4:p.Gly393=
ENST00000262464.8:c.1179C>T ENSP00000262464.4:p.Gly393=
ENST00000508053.5:c.1179C>T ENSP00000424571.1:p.Gly393=
ENST00000508989.5:c.1080C>T ENSP00000425596.1:p.Gly360=
ENST00000619499.4:c.1176C>T ENSP00000482132.1:p.Gly392=
NM_001999.3:c.1179C>T NP_001990.2:p.Gly393=
XM_017009228.2:c.1079-1806C>T XP_016864717.1:n.1079-1806C>T
NM_001999.4:c.1179C>T MANE Select NP_001990.2:p.Gly393=