Canonical Allele Identifier: CA446310163

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127671226C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335534C>T , CM000667.2:g.128335534C>T	GRCh38
NC_000005.9:g.127671226C>T , CM000667.1:g.127671226C>T	GRCh37
NC_000005.8:g.127699125C>T	NCBI36
NG_008750.1:g.207510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.552G>A
ENST00000703785.1:n.633G>A
ENST00000262464.9:c.3768G>A MANE Select	ENSP00000262464.4:p.Gln1256=
ENST00000262464.8:c.3768G>A	ENSP00000262464.4:p.Gln1256=
ENST00000507835.5:c.318G>A	ENSP00000426839.1:p.Gln106=
ENST00000508053.5:c.3768G>A	ENSP00000424571.1:p.Gln1256=
ENST00000508989.5:c.3669G>A	ENSP00000425596.1:p.Gln1223=
ENST00000619499.4:c.3765G>A	ENSP00000482132.1:p.Gln1255=
NM_001999.3:c.3768G>A	NP_001990.2:p.Gln1256=
XM_017009228.2:c.3615G>A	XP_016864717.1:p.Gln1205=
NM_001999.4:c.3768G>A MANE Select	NP_001990.2:p.Gln1256=