Canonical Allele Identifier: CA360759474

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127673781C>G (hg19) ; chr5:g.128338089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338089C>G , CM000667.2:g.128338089C>G	GRCh38
NC_000005.9:g.127673781C>G , CM000667.1:g.127673781C>G	GRCh37
NC_000005.8:g.127701680C>G	NCBI36
NG_008750.1:g.204955G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.290G>C
ENST00000703785.1:n.371G>C
ENST00000262464.9:c.3506G>C MANE Select	ENSP00000262464.4:p.Cys1169Ser
ENST00000262464.8:c.3506G>C	ENSP00000262464.4:p.Cys1169Ser
ENST00000507835.5:c.56G>C	ENSP00000426839.1:p.Cys19Ser
ENST00000508053.5:c.3506G>C	ENSP00000424571.1:p.Cys1169Ser
ENST00000508989.5:c.3407G>C	ENSP00000425596.1:p.Cys1136Ser
ENST00000619499.4:c.3503G>C	ENSP00000482132.1:p.Cys1168Ser
NM_001999.3:c.3506G>C	NP_001990.2:p.Cys1169Ser
XM_017009228.2:c.3353G>C	XP_016864717.1:p.Cys1118Ser
NM_001999.4:c.3506G>C MANE Select	NP_001990.2:p.Cys1169Ser