Canonical Allele Identifier: CA446309517

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668668A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332976A>G , CM000667.2:g.128332976A>G	GRCh38
NC_000005.9:g.127668668A>G , CM000667.1:g.127668668A>G	GRCh37
NC_000005.8:g.127696567A>G	NCBI36
NG_008750.1:g.210068T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.942T>C
ENST00000703785.1:n.1023T>C
ENST00000262464.9:c.4158T>C MANE Select	ENSP00000262464.4:p.Asn1386=
ENST00000262464.8:c.4158T>C	ENSP00000262464.4:p.Asn1386=
ENST00000507835.5:c.708T>C	ENSP00000426839.1:p.Asn236=
ENST00000508053.5:c.4158T>C	ENSP00000424571.1:p.Asn1386=
ENST00000508989.5:c.4059T>C	ENSP00000425596.1:p.Asn1353=
ENST00000619499.4:c.4155T>C	ENSP00000482132.1:p.Asn1385=
NM_001999.3:c.4158T>C	NP_001990.2:p.Asn1386=
XM_017009228.2:c.4005T>C	XP_016864717.1:p.Asn1335=
NM_001999.4:c.4158T>C MANE Select	NP_001990.2:p.Asn1386=