Canonical Allele Identifier: CA360754740

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668629C>G (hg19) ; chr5:g.128332937C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332937C>G , CM000667.2:g.128332937C>G	GRCh38
NC_000005.9:g.127668629C>G , CM000667.1:g.127668629C>G	GRCh37
NC_000005.8:g.127696528C>G	NCBI36
NG_008750.1:g.210107G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.981G>C
ENST00000703785.1:n.1062G>C
ENST00000262464.9:c.4197G>C MANE Select	ENSP00000262464.4:p.Trp1399Cys
ENST00000262464.8:c.4197G>C	ENSP00000262464.4:p.Trp1399Cys
ENST00000507835.5:c.747G>C	ENSP00000426839.1:p.Trp249Cys
ENST00000508053.5:c.4197G>C	ENSP00000424571.1:p.Trp1399Cys
ENST00000508989.5:c.4098G>C	ENSP00000425596.1:p.Trp1366Cys
ENST00000619499.4:c.4194G>C	ENSP00000482132.1:p.Trp1398Cys
NM_001999.3:c.4197G>C	NP_001990.2:p.Trp1399Cys
XM_017009228.2:c.4044G>C	XP_016864717.1:p.Trp1348Cys
NM_001999.4:c.4197G>C MANE Select	NP_001990.2:p.Trp1399Cys