Canonical Allele Identifier: CA446310855

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127674719A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128339027A>G , CM000667.2:g.128339027A>G	GRCh38
NC_000005.9:g.127674719A>G , CM000667.1:g.127674719A>G	GRCh37
NC_000005.8:g.127702618A>G	NCBI36
NG_008750.1:g.204017T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.162T>C
ENST00000703785.1:n.243T>C
ENST00000262464.9:c.3378T>C MANE Select	ENSP00000262464.4:p.Cys1126=
ENST00000262464.8:c.3378T>C	ENSP00000262464.4:p.Cys1126=
ENST00000507835.5:c.-73T>C	ENSP00000426839.1:n.-73T>C
ENST00000508053.5:c.3378T>C	ENSP00000424571.1:p.Cys1126=
ENST00000508989.5:c.3279T>C	ENSP00000425596.1:p.Cys1093=
ENST00000619499.4:c.3375T>C	ENSP00000482132.1:p.Cys1125=
NM_001999.3:c.3378T>C	NP_001990.2:p.Cys1126=
XM_017009228.2:c.3225T>C	XP_016864717.1:p.Cys1075=
NM_001999.4:c.3378T>C MANE Select	NP_001990.2:p.Cys1126=