Canonical Allele Identifier: CA617832390

Gene: FBN1

Linked Data

• dbSNP Id: rs1215350102
• gnomAD v2: 15-48703620-C-T
• gnomAD v4: 15-48411423-C-T
• MyVariant Identifiers: chr15:g.48703620C>T (hg19) ; chr15:g.48411423C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411423C>T , CM000677.2:g.48411423C>T	GRCh38
NC_000015.9:g.48703620C>T , CM000677.1:g.48703620C>T	GRCh37
NC_000015.8:g.46490912C>T	NCBI36
NG_008805.2:g.239366G>A , LRG_778:g.239366G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1035-44G>A	ENSP00000453958.2:n.*1035-44G>A
ENST00000674301.2:c.*1740-44G>A	ENSP00000501333.2:n.*1740-44G>A
ENST00000682158.1:n.1608-44G>A
ENST00000682170.1:n.2408-44G>A
ENST00000682767.1:n.1524-44G>A
ENST00000316623.10:c.8227-44G>A MANE Select	ENSP00000325527.5:n.8227-44G>A
ENST00000674301.1:c.3393-44G>A	ENSP00000501333.1:n.3393-44G>A
ENST00000316623.9:c.8227-44G>A	ENSP00000325527.5:n.8227-44G>A
ENST00000559133.5:c.3596-44G>A
ENST00000561429.1:n.482-44G>A
NM_000138.4:c.8227-44G>A , LRG_778t1:c.8227-44G>A	NP_000129.3:n.8227-44G>A
NM_000138.5:c.8227-44G>A MANE Select	NP_000129.3:n.8227-44G>A