Canonical Allele Identifier: CA360758076

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127671230G>T (hg19) ; chr5:g.128335538G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335538G>T , CM000667.2:g.128335538G>T	GRCh38
NC_000005.9:g.127671230G>T , CM000667.1:g.127671230G>T	GRCh37
NC_000005.8:g.127699129G>T	NCBI36
NG_008750.1:g.207506C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.548C>A
ENST00000703785.1:n.629C>A
ENST00000262464.9:c.3764C>A MANE Select	ENSP00000262464.4:p.Thr1255Asn
ENST00000262464.8:c.3764C>A	ENSP00000262464.4:p.Thr1255Asn
ENST00000507835.5:c.314C>A	ENSP00000426839.1:p.Thr105Asn
ENST00000508053.5:c.3764C>A	ENSP00000424571.1:p.Thr1255Asn
ENST00000508989.5:c.3665C>A	ENSP00000425596.1:p.Thr1222Asn
ENST00000619499.4:c.3761C>A	ENSP00000482132.1:p.Thr1254Asn
NM_001999.3:c.3764C>A	NP_001990.2:p.Thr1255Asn
XM_017009228.2:c.3611C>A	XP_016864717.1:p.Thr1204Asn
NM_001999.4:c.3764C>A MANE Select	NP_001990.2:p.Thr1255Asn