Canonical Allele Identifier: CA015004

Gene: FBN1

Linked Data

• ClinVar Variation Id: 42357
• ClinVar RCV Id: RCV000035196
• dbSNP Id: rs397515805
• MyVariant Identifiers: chr15:g.48762923C>T (hg19) ; chr15:g.48470726C>T (hg38)
• PubMed: PMID:1301946 ; PMID:19293843 ; PMID:24793577

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48470726C>T , CM000677.2:g.48470726C>T	GRCh38
NC_000015.9:g.48762923C>T , CM000677.1:g.48762923C>T	GRCh37
NC_000015.8:g.46550215C>T	NCBI36
NG_008805.2:g.180063G>A , LRG_778:g.180063G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.4367G>A	ENSP00000453958.2:p.Cys1456Tyr
ENST00000674301.2:c.4367G>A	ENSP00000501333.2:p.Cys1456Tyr
ENST00000683268.1:n.334G>A
ENST00000684448.1:n.3041G>A
ENST00000316623.10:c.4367G>A MANE Select	ENSP00000325527.5:p.Cys1456Tyr
ENST00000316623.9:c.4367G>A	ENSP00000325527.5:p.Cys1456Tyr
ENST00000537463.6:c.*130G>A	ENSP00000440294.2:n.*130G>A
NM_000138.4:c.4367G>A , LRG_778t1:c.4367G>A	NP_000129.3:p.Cys1456Tyr
NM_000138.5:c.4367G>A MANE Select	NP_000129.3:p.Cys1456Tyr