Canonical Allele Identifier: CA446310634

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127673756A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338064A>C , CM000667.2:g.128338064A>C	GRCh38
NC_000005.9:g.127673756A>C , CM000667.1:g.127673756A>C	GRCh37
NC_000005.8:g.127701655A>C	NCBI36
NG_008750.1:g.204980T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.315T>G
ENST00000703785.1:n.396T>G
ENST00000262464.9:c.3531T>G MANE Select	ENSP00000262464.4:p.Thr1177=
ENST00000262464.8:c.3531T>G	ENSP00000262464.4:p.Thr1177=
ENST00000507835.5:c.81T>G	ENSP00000426839.1:p.Thr27=
ENST00000508053.5:c.3531T>G	ENSP00000424571.1:p.Thr1177=
ENST00000508989.5:c.3432T>G	ENSP00000425596.1:p.Thr1144=
ENST00000619499.4:c.3528T>G	ENSP00000482132.1:p.Thr1176=
NM_001999.3:c.3531T>G	NP_001990.2:p.Thr1177=
XM_017009228.2:c.3378T>G	XP_016864717.1:p.Thr1126=
NM_001999.4:c.3531T>G MANE Select	NP_001990.2:p.Thr1177=