Canonical Allele Identifier: CA3395496

Gene: FBN2

Linked Data

• dbSNP Id: rs560259673
• ExAC: 5:127693082 T / C
• gnomAD v3: 5-128357390-T-C
• gnomAD v4: 5-128357390-T-C
• MyVariant Identifiers: chr5:g.127693082T>C (hg19) ; chr5:g.128357390T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357390T>C , CM000667.2:g.128357390T>C	GRCh38
NC_000005.9:g.127693082T>C , CM000667.1:g.127693082T>C	GRCh37
NC_000005.8:g.127720981T>C	NCBI36
NG_008750.1:g.185654A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2560A>G MANE Select	ENSP00000262464.4:p.Asn854Asp
ENST00000262464.8:c.2560A>G	ENSP00000262464.4:p.Asn854Asp
ENST00000508053.5:c.2560A>G	ENSP00000424571.1:p.Asn854Asp
ENST00000508989.5:c.2461A>G	ENSP00000425596.1:p.Asn821Asp
ENST00000619499.4:c.2557A>G	ENSP00000482132.1:p.Asn853Asp
NM_001999.3:c.2560A>G	NP_001990.2:p.Asn854Asp
XM_017009228.2:c.2407A>G	XP_016864717.1:p.Asn803Asp
NM_001999.4:c.2560A>G MANE Select	NP_001990.2:p.Asn854Asp