Canonical Allele Identifier: CA3395243

Gene: FBN2

Linked Data

• dbSNP Id: rs749270790
• ExAC: 5:127674681 T / C
• gnomAD v4: 5-128338989-T-C
• MyVariant Identifiers: chr5:g.127674681T>C (hg19) ; chr5:g.128338989T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338989T>C , CM000667.2:g.128338989T>C	GRCh38
NC_000005.9:g.127674681T>C , CM000667.1:g.127674681T>C	GRCh37
NC_000005.8:g.127702580T>C	NCBI36
NG_008750.1:g.204055A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.200A>G
ENST00000703785.1:n.281A>G
ENST00000262464.9:c.3416A>G MANE Select	ENSP00000262464.4:p.Glu1139Gly
ENST00000262464.8:c.3416A>G	ENSP00000262464.4:p.Glu1139Gly
ENST00000507835.5:c.-35A>G	ENSP00000426839.1:n.-35A>G
ENST00000508053.5:c.3416A>G	ENSP00000424571.1:p.Glu1139Gly
ENST00000508989.5:c.3317A>G	ENSP00000425596.1:p.Glu1106Gly
ENST00000619499.4:c.3413A>G	ENSP00000482132.1:p.Glu1138Gly
NM_001999.3:c.3416A>G	NP_001990.2:p.Glu1139Gly
XM_017009228.2:c.3263A>G	XP_016864717.1:p.Glu1088Gly
NM_001999.4:c.3416A>G MANE Select	NP_001990.2:p.Glu1139Gly