Canonical Allele Identifier: CA1081376639

Gene: FBN2

Linked Data

• dbSNP Id: rs1350874176
• gnomAD v3: 5-128528068-A-G
• gnomAD v4: 5-128528068-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128528068A>G , CM000667.2:g.128528068A>G	GRCh38
NC_000005.9:g.127863761A>G , CM000667.1:g.127863761A>G	GRCh37
NC_000005.8:g.127891660A>G	NCBI36
NG_008750.1:g.14975T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508053.6:c.437-101T>C	ENSP00000424571.2:n.437-101T>C
ENST00000703787.1:n.144-101T>C
ENST00000262464.9:c.437-101T>C MANE Select	ENSP00000262464.4:n.437-101T>C
ENST00000262464.8:c.437-101T>C	ENSP00000262464.4:n.437-101T>C
ENST00000502468.5:c.437-101T>C	ENSP00000424753.1:n.437-101T>C
ENST00000508053.5:c.437-101T>C	ENSP00000424571.1:n.437-101T>C
ENST00000508989.5:c.338-101T>C	ENSP00000425596.1:n.338-101T>C
ENST00000514742.1:n.1057-101T>C
ENST00000619499.4:c.437-101T>C	ENSP00000482132.1:n.437-101T>C
ENST00000620257.1:c.437-101T>C	ENSP00000479157.1:n.437-101T>C
NM_001999.3:c.437-101T>C	NP_001990.2:n.437-101T>C
XM_017009228.2:c.437-101T>C	XP_016864717.1:n.437-101T>C
NM_001999.4:c.437-101T>C MANE Select	NP_001990.2:n.437-101T>C