Canonical Allele Identifier: CA446310359

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127671681T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335989T>C , CM000667.2:g.128335989T>C	GRCh38
NC_000005.9:g.127671681T>C , CM000667.1:g.127671681T>C	GRCh37
NC_000005.8:g.127699580T>C	NCBI36
NG_008750.1:g.207055A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.507A>G
ENST00000703785.1:n.588A>G
ENST00000262464.9:c.3723A>G MANE Select	ENSP00000262464.4:p.Thr1241=
ENST00000262464.8:c.3723A>G	ENSP00000262464.4:p.Thr1241=
ENST00000507835.5:c.273A>G	ENSP00000426839.1:p.Thr91=
ENST00000508053.5:c.3723A>G	ENSP00000424571.1:p.Thr1241=
ENST00000508989.5:c.3624A>G	ENSP00000425596.1:p.Thr1208=
ENST00000619499.4:c.3720A>G	ENSP00000482132.1:p.Thr1240=
NM_001999.3:c.3723A>G	NP_001990.2:p.Thr1241=
XM_017009228.2:c.3570A>G	XP_016864717.1:p.Thr1190=
NM_001999.4:c.3723A>G MANE Select	NP_001990.2:p.Thr1241=