Canonical Allele Identifier: CA446308962

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127873171C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128537478C>G , CM000667.2:g.128537478C>G	GRCh38
NC_000005.9:g.127873171C>G , CM000667.1:g.127873171C>G	GRCh37
NC_000005.8:g.127901070C>G	NCBI36
NG_008750.1:g.5565G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000508053.6:c.126G>C	ENSP00000424571.2:p.Pro42=
ENST00000262464.9:c.126G>C MANE Select	ENSP00000262464.4:p.Pro42=
ENST00000262464.8:c.126G>C	ENSP00000262464.4:p.Pro42=
ENST00000502468.5:c.126G>C	ENSP00000424753.1:p.Pro42=
ENST00000508053.5:c.126G>C	ENSP00000424571.1:p.Pro42=
ENST00000508989.5:c.126G>C	ENSP00000425596.1:p.Pro42=
ENST00000514742.1:n.746G>C
ENST00000619499.4:c.126G>C	ENSP00000482132.1:p.Pro42=
ENST00000620257.1:c.126G>C	ENSP00000479157.1:p.Pro42=
NM_001999.3:c.126G>C	NP_001990.2:p.Pro42=
XM_017009228.2:c.126G>C	XP_016864717.1:p.Pro42=
NM_001999.4:c.126G>C MANE Select	NP_001990.2:p.Pro42=