Canonical Allele Identifier: CA490118955

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703429T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411232T>G , CM000677.2:g.48411232T>G	GRCh38
NC_000015.9:g.48703429T>G , CM000677.1:g.48703429T>G	GRCh37
NC_000015.8:g.46490721T>G	NCBI36
NG_008805.2:g.239557A>C , LRG_778:g.239557A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1182A>C	ENSP00000453958.2:n.*1182A>C
ENST00000674301.2:c.*1887A>C	ENSP00000501333.2:n.*1887A>C
ENST00000682158.1:n.1755A>C
ENST00000682170.1:n.2555A>C
ENST00000682767.1:n.1671A>C
ENST00000316623.10:c.8374A>C MANE Select	ENSP00000325527.5:p.Arg2792=
ENST00000674301.1:c.3540A>C	ENSP00000501333.1:n.3540A>C
ENST00000316623.9:c.8374A>C	ENSP00000325527.5:p.Arg2792=
ENST00000559133.5:c.3743A>C
ENST00000561429.1:n.629A>C
NM_000138.4:c.8374A>C , LRG_778t1:c.8374A>C	NP_000129.3:p.Arg2792=
NM_000138.5:c.8374A>C MANE Select	NP_000129.3:p.Arg2792=