Canonical Allele Identifier: CA2675114178

Gene: FBN2

Linked Data

• gnomAD v4: 5-128301235-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128301239del , CM000667.2:g.128301239del	GRCh38
NC_000005.9:g.127636931del , CM000667.1:g.127636931del	GRCh37
NC_000005.8:g.127664830del	NCBI36
NG_008750.1:g.241808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.2830+146del
ENST00000703785.1:n.2749+146del
ENST00000262464.9:c.6046+146del MANE Select	ENSP00000262464.4:n.6046+146del
ENST00000262464.8:c.6046+146del	ENSP00000262464.4:n.6046+146del
ENST00000508053.5:c.6046+146del	ENSP00000424571.1:n.6046+146del
ENST00000619499.4:c.6043+146del	ENSP00000482132.1:n.6043+146del
NM_001999.3:c.6046+146del	NP_001990.2:n.6046+146del
XM_017009228.2:c.5893+146del	XP_016864717.1:n.5893+146del
NM_001999.4:c.6046+146del MANE Select	NP_001990.2:n.6046+146del