Canonical Allele Identifier: CA360757485

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127670952C>A (hg19) ; chr5:g.128335260C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335260C>A , CM000667.2:g.128335260C>A	GRCh38
NC_000005.9:g.127670952C>A , CM000667.1:g.127670952C>A	GRCh37
NC_000005.8:g.127698851C>A	NCBI36
NG_008750.1:g.207784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.667G>T
ENST00000703785.1:n.748G>T
ENST00000262464.9:c.3883G>T MANE Select	ENSP00000262464.4:p.Asp1295Tyr
ENST00000262464.8:c.3883G>T	ENSP00000262464.4:p.Asp1295Tyr
ENST00000507835.5:c.433G>T	ENSP00000426839.1:p.Asp145Tyr
ENST00000508053.5:c.3883G>T	ENSP00000424571.1:p.Asp1295Tyr
ENST00000508989.5:c.3784G>T	ENSP00000425596.1:p.Asp1262Tyr
ENST00000619499.4:c.3880G>T	ENSP00000482132.1:p.Asp1294Tyr
NM_001999.3:c.3883G>T	NP_001990.2:p.Asp1295Tyr
XM_017009228.2:c.3730G>T	XP_016864717.1:p.Asp1244Tyr
NM_001999.4:c.3883G>T MANE Select	NP_001990.2:p.Asp1295Tyr