Canonical Allele Identifier: CA2175508306

Gene: FBN1

Linked Data

• dbSNP Id: rs2043114891

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441500G>A , CM000677.2:g.48441500G>A	GRCh38
NC_000015.9:g.48733697G>A , CM000677.1:g.48733697G>A	GRCh37
NC_000015.8:g.46520989G>A	NCBI36
NG_008805.2:g.209289C>T , LRG_778:g.209289C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6163+221C>T	ENSP00000453958.2:n.6163+221C>T
ENST00000674301.2:c.6163+221C>T	ENSP00000501333.2:n.6163+221C>T
ENST00000316623.10:c.6163+221C>T MANE Select	ENSP00000325527.5:n.6163+221C>T
ENST00000674301.1:c.1162+221C>T	ENSP00000501333.1:n.1162+221C>T
ENST00000316623.9:c.6163+221C>T	ENSP00000325527.5:n.6163+221C>T
ENST00000537463.6:c.*1926+221C>T	ENSP00000440294.2:n.*1926+221C>T
ENST00000559133.5:c.1470+221C>T
ENST00000560820.1:n.283+221C>T
NM_000138.4:c.6163+221C>T , LRG_778t1:c.6163+221C>T	NP_000129.3:n.6163+221C>T
NM_000138.5:c.6163+221C>T MANE Select	NP_000129.3:n.6163+221C>T