Canonical Allele Identifier: CA360754791

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668635T>G (hg19) ; chr5:g.128332943T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332943T>G , CM000667.2:g.128332943T>G	GRCh38
NC_000005.9:g.127668635T>G , CM000667.1:g.127668635T>G	GRCh37
NC_000005.8:g.127696534T>G	NCBI36
NG_008750.1:g.210101A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.975A>C
ENST00000703785.1:n.1056A>C
ENST00000262464.9:c.4191A>C MANE Select	ENSP00000262464.4:p.Glu1397Asp
ENST00000262464.8:c.4191A>C	ENSP00000262464.4:p.Glu1397Asp
ENST00000507835.5:c.741A>C	ENSP00000426839.1:p.Glu247Asp
ENST00000508053.5:c.4191A>C	ENSP00000424571.1:p.Glu1397Asp
ENST00000508989.5:c.4092A>C	ENSP00000425596.1:p.Glu1364Asp
ENST00000619499.4:c.4188A>C	ENSP00000482132.1:p.Glu1396Asp
NM_001999.3:c.4191A>C	NP_001990.2:p.Glu1397Asp
XM_017009228.2:c.4038A>C	XP_016864717.1:p.Glu1346Asp
NM_001999.4:c.4191A>C MANE Select	NP_001990.2:p.Glu1397Asp