Canonical Allele Identifier: CA2675120642

Gene: FBN2

Linked Data

• gnomAD v4: 5-128394997-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128394997G>A , CM000667.2:g.128394997G>A	GRCh38
NC_000005.9:g.127730690G>A , CM000667.1:g.127730690G>A	GRCh37
NC_000005.8:g.127758589G>A	NCBI36
NG_008750.1:g.148046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703787.1:n.938+125C>T
ENST00000262464.9:c.1231+125C>T MANE Select	ENSP00000262464.4:n.1231+125C>T
ENST00000262464.8:c.1231+125C>T	ENSP00000262464.4:n.1231+125C>T
ENST00000508053.5:c.1231+125C>T	ENSP00000424571.1:n.1231+125C>T
ENST00000508989.5:c.1132+125C>T	ENSP00000425596.1:n.1132+125C>T
ENST00000619499.4:c.1228+125C>T	ENSP00000482132.1:n.1228+125C>T
NM_001999.3:c.1231+125C>T	NP_001990.2:n.1231+125C>T
XM_017009228.2:c.1079-1629C>T	XP_016864717.1:n.1079-1629C>T
NM_001999.4:c.1231+125C>T MANE Select	NP_001990.2:n.1231+125C>T