Canonical Allele Identifier: CA360757847

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127670975C>A (hg19) ; chr5:g.128335283C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335283C>A , CM000667.2:g.128335283C>A	GRCh38
NC_000005.9:g.127670975C>A , CM000667.1:g.127670975C>A	GRCh37
NC_000005.8:g.127698874C>A	NCBI36
NG_008750.1:g.207761G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.644G>T
ENST00000703785.1:n.725G>T
ENST00000262464.9:c.3860G>T MANE Select	ENSP00000262464.4:p.Cys1287Phe
ENST00000262464.8:c.3860G>T	ENSP00000262464.4:p.Cys1287Phe
ENST00000507835.5:c.410G>T	ENSP00000426839.1:p.Cys137Phe
ENST00000508053.5:c.3860G>T	ENSP00000424571.1:p.Cys1287Phe
ENST00000508989.5:c.3761G>T	ENSP00000425596.1:p.Cys1254Phe
ENST00000619499.4:c.3857G>T	ENSP00000482132.1:p.Cys1286Phe
NM_001999.3:c.3860G>T	NP_001990.2:p.Cys1287Phe
XM_017009228.2:c.3707G>T	XP_016864717.1:p.Cys1236Phe
NM_001999.4:c.3860G>T MANE Select	NP_001990.2:p.Cys1287Phe