Canonical Allele Identifier: CA392333153

Gene: FBN1

Linked Data

• ClinVar Variation Id: 16436
• ClinVar RCV Id: RCV000017898
• dbSNP Id: rs869025419
• MyVariant Identifiers: chr15:g.48725062C>G (hg19) ; chr15:g.48432865C>G (hg38)
• PubMed: PMID:8101042 ; PMID:8750301

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48432865C>G , CM000677.2:g.48432865C>G	GRCh38
NC_000015.9:g.48725062C>G , CM000677.1:g.48725062C>G	GRCh37
NC_000015.8:g.46512354C>G	NCBI36
NG_008805.2:g.217924G>C , LRG_778:g.217924G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6739+1G>C	ENSP00000453958.2:n.6739+1G>C
ENST00000674301.2:c.*190+1G>C	ENSP00000501333.2:n.*190+1G>C
ENST00000682170.1:n.348+1G>C
ENST00000316623.10:c.6739+1G>C MANE Select	ENSP00000325527.5:n.6739+1G>C
ENST00000674301.1:c.1843+1G>C	ENSP00000501333.1:n.1843+1G>C
ENST00000316623.9:c.6739+1G>C	ENSP00000325527.5:n.6739+1G>C
ENST00000537463.6:c.*2502+1G>C	ENSP00000440294.2:n.*2502+1G>C
ENST00000559133.5:c.2046+1G>C
ENST00000560720.1:n.26+1G>C
NM_000138.4:c.6739+1G>C , LRG_778t1:c.6739+1G>C	NP_000129.3:n.6739+1G>C
NM_000138.5:c.6739+1G>C MANE Select	NP_000129.3:n.6739+1G>C