Canonical Allele Identifier: CA360757540

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127670968G>C (hg19) ; chr5:g.128335276G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335276G>C , CM000667.2:g.128335276G>C	GRCh38
NC_000005.9:g.127670968G>C , CM000667.1:g.127670968G>C	GRCh37
NC_000005.8:g.127698867G>C	NCBI36
NG_008750.1:g.207768C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.651C>G
ENST00000703785.1:n.732C>G
ENST00000262464.9:c.3867C>G MANE Select	ENSP00000262464.4:p.Asn1289Lys
ENST00000262464.8:c.3867C>G	ENSP00000262464.4:p.Asn1289Lys
ENST00000507835.5:c.417C>G	ENSP00000426839.1:p.Asn139Lys
ENST00000508053.5:c.3867C>G	ENSP00000424571.1:p.Asn1289Lys
ENST00000508989.5:c.3768C>G	ENSP00000425596.1:p.Asn1256Lys
ENST00000619499.4:c.3864C>G	ENSP00000482132.1:p.Asn1288Lys
NM_001999.3:c.3867C>G	NP_001990.2:p.Asn1289Lys
XM_017009228.2:c.3714C>G	XP_016864717.1:p.Asn1238Lys
NM_001999.4:c.3867C>G MANE Select	NP_001990.2:p.Asn1289Lys