Canonical Allele Identifier: CA16606697

Gene: FBN1

Linked Data

• ClinVar Variation Id: 379519
• ClinVar RCV Id: RCV000422144 ; RCV003766214
• dbSNP Id: rs113453570
• MyVariant Identifiers: chr15:g.48729517A>G (hg19) ; chr15:g.48437320A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48437320A>G , CM000677.2:g.48437320A>G	GRCh38
NC_000015.9:g.48729517A>G , CM000677.1:g.48729517A>G	GRCh37
NC_000015.8:g.46516809A>G	NCBI36
NG_008805.2:g.213469T>C , LRG_778:g.213469T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6379+2T>C	ENSP00000453958.2:n.6379+2T>C
ENST00000674301.2:c.6379+2T>C	ENSP00000501333.2:n.6379+2T>C
ENST00000316623.10:c.6379+2T>C MANE Select	ENSP00000325527.5:n.6379+2T>C
ENST00000674301.1:c.1378+2T>C	ENSP00000501333.1:n.1378+2T>C
ENST00000316623.9:c.6379+2T>C	ENSP00000325527.5:n.6379+2T>C
ENST00000537463.6:c.*2142+2T>C	ENSP00000440294.2:n.*2142+2T>C
ENST00000559133.5:c.1686+2T>C
NM_000138.4:c.6379+2T>C , LRG_778t1:c.6379+2T>C	NP_000129.3:n.6379+2T>C
NM_000138.5:c.6379+2T>C MANE Select	NP_000129.3:n.6379+2T>C