Canonical Allele Identifier: CA3395870

Gene: FBN2

Linked Data

• ClinVar Variation Id: 411830
• ClinVar RCV Id: RCV000474036 ; RCV001764448
• dbSNP Id: rs371826887
• ExAC: 5:127730895 G / A
• gnomAD v2: 5-127730895-G-A
• gnomAD v3: 5-128395202-G-A
• gnomAD v4: 5-128395202-G-A
• COSMIC: COSM3927454 ; COSM3927455
• MyVariant Identifiers: chr5:g.127730895G>A (hg19) ; chr5:g.128395202G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128395202G>A , CM000667.2:g.128395202G>A	GRCh38
NC_000005.9:g.127730895G>A , CM000667.1:g.127730895G>A	GRCh37
NC_000005.8:g.127758794G>A	NCBI36
NG_008750.1:g.147841C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703787.1:n.858C>T
ENST00000262464.9:c.1151C>T MANE Select	ENSP00000262464.4:p.Thr384Met
ENST00000262464.8:c.1151C>T	ENSP00000262464.4:p.Thr384Met
ENST00000508053.5:c.1151C>T	ENSP00000424571.1:p.Thr384Met
ENST00000508989.5:c.1052C>T	ENSP00000425596.1:p.Thr351Met
ENST00000619499.4:c.1148C>T	ENSP00000482132.1:p.Thr383Met
NM_001999.3:c.1151C>T	NP_001990.2:p.Thr384Met
XM_017009228.2:c.1079-1834C>T	XP_016864717.1:n.1079-1834C>T
NM_001999.4:c.1151C>T MANE Select	NP_001990.2:p.Thr384Met