Canonical Allele Identifier: CA2675117856

Gene: FBN2

Linked Data

• gnomAD v4: 5-128339173-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128339176del , CM000667.2:g.128339176del	GRCh38
NC_000005.9:g.127674868del , CM000667.1:g.127674868del	GRCh37
NC_000005.8:g.127702767del	NCBI36
NG_008750.1:g.203870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.15del
ENST00000703785.1:n.96del
ENST00000262464.9:c.3344-113del MANE Select	ENSP00000262464.4:n.3344-113del
ENST00000262464.8:c.3344-113del	ENSP00000262464.4:n.3344-113del
ENST00000507835.5:c.-220del	ENSP00000426839.1:n.-220del
ENST00000508053.5:c.3344-113del	ENSP00000424571.1:n.3344-113del
ENST00000508989.5:c.3245-113del	ENSP00000425596.1:n.3245-113del
ENST00000619499.4:c.3341-113del	ENSP00000482132.1:n.3341-113del
NM_001999.3:c.3344-113del	NP_001990.2:n.3344-113del
XM_017009228.2:c.3191-113del	XP_016864717.1:n.3191-113del
NM_001999.4:c.3344-113del MANE Select	NP_001990.2:n.3344-113del