Canonical Allele Identifier: CA360754067

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127666331T>C (hg19) ; chr5:g.128330639T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330639T>C , CM000667.2:g.128330639T>C	GRCh38
NC_000005.9:g.127666331T>C , CM000667.1:g.127666331T>C	GRCh37
NC_000005.8:g.127694230T>C	NCBI36
NG_008750.1:g.212405A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1063A>G
ENST00000703785.1:n.1144A>G
ENST00000262464.9:c.4279A>G MANE Select	ENSP00000262464.4:p.Asn1427Asp
ENST00000262464.8:c.4279A>G	ENSP00000262464.4:p.Asn1427Asp
ENST00000507835.5:c.829A>G	ENSP00000426839.1:p.Asn277Asp
ENST00000508053.5:c.4279A>G	ENSP00000424571.1:p.Asn1427Asp
ENST00000508989.5:c.4180A>G	ENSP00000425596.1:p.Asn1394Asp
ENST00000619499.4:c.4276A>G	ENSP00000482132.1:p.Asn1426Asp
NM_001999.3:c.4279A>G	NP_001990.2:p.Asn1427Asp
XM_017009228.2:c.4126A>G	XP_016864717.1:p.Asn1376Asp
NM_001999.4:c.4279A>G MANE Select	NP_001990.2:p.Asn1427Asp