Canonical Allele Identifier: CA803626462

Gene: FBN2

Linked Data

• dbSNP Id: rs1301041643
• gnomAD v3: 5-128300398-CT-C
• gnomAD v4: 5-128300398-CT-C
• MyVariant Identifiers: chr5:g.127636091del (hg19) ; chr5:g.128300399del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128300400del , CM000667.2:g.128300400del	GRCh38
NC_000005.9:g.127636092del , CM000667.1:g.127636092del	GRCh37
NC_000005.8:g.127663991del	NCBI36
NG_008750.1:g.242645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.2950+418del
ENST00000703785.1:n.2869+418del
ENST00000262464.9:c.6166+418del MANE Select	ENSP00000262464.4:n.6166+418del
ENST00000262464.8:c.6166+418del	ENSP00000262464.4:n.6166+418del
ENST00000508053.5:c.6166+418del	ENSP00000424571.1:n.6166+418del
ENST00000619499.4:c.6163+418del	ENSP00000482132.1:n.6163+418del
NM_001999.3:c.6166+418del	NP_001990.2:n.6166+418del
XM_017009228.2:c.6013+418del	XP_016864717.1:n.6013+418del
NM_001999.4:c.6166+418del MANE Select	NP_001990.2:n.6166+418del