Canonical Allele Identifier: CA2580089693

Gene: FBN1

Linked Data

• ClinVar Variation Id: 2069111
• ClinVar RCV Id: RCV002961906

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428478G>A , CM000677.2:g.48428478G>A	GRCh38
NC_000015.9:g.48720675G>A , CM000677.1:g.48720675G>A	GRCh37
NC_000015.8:g.46507967G>A	NCBI36
NG_008805.2:g.222311C>T , LRG_778:g.222311C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6872-7C>T	ENSP00000453958.2:n.6872-7C>T
ENST00000674301.2:c.*323-7C>T	ENSP00000501333.2:n.*323-7C>T
ENST00000682170.1:n.481-7C>T
ENST00000682767.1:n.100C>T
ENST00000316623.10:c.6872-7C>T MANE Select	ENSP00000325527.5:n.6872-7C>T
ENST00000674301.1:c.1976-7C>T	ENSP00000501333.1:n.1976-7C>T
ENST00000316623.9:c.6872-7C>T	ENSP00000325527.5:n.6872-7C>T
ENST00000559133.5:c.2179-7C>T
ENST00000560720.1:n.159-7C>T
NM_000138.4:c.6872-7C>T , LRG_778t1:c.6872-7C>T	NP_000129.3:n.6872-7C>T
NM_000138.5:c.6872-7C>T MANE Select	NP_000129.3:n.6872-7C>T