Canonical Allele Identifier: CA618009216

Gene: FBN1

Linked Data

• dbSNP Id: rs1256996024
• gnomAD v2: 15-48713906-A-G
• gnomAD v4: 15-48421709-A-G
• MyVariant Identifiers: chr15:g.48713906A>G (hg19) ; chr15:g.48421709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421709A>G , CM000677.2:g.48421709A>G	GRCh38
NC_000015.9:g.48713906A>G , CM000677.1:g.48713906A>G	GRCh37
NC_000015.8:g.46501198A>G	NCBI36
NG_008805.2:g.229080T>C , LRG_778:g.229080T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*379-23T>C	ENSP00000453958.2:n.*379-23T>C
ENST00000674301.2:c.*1084-23T>C	ENSP00000501333.2:n.*1084-23T>C
ENST00000682170.1:n.1752-23T>C
ENST00000682767.1:n.868-23T>C
ENST00000316623.10:c.7571-23T>C MANE Select	ENSP00000325527.5:n.7571-23T>C
ENST00000674301.1:c.2737-23T>C	ENSP00000501333.1:n.2737-23T>C
ENST00000316623.9:c.7571-23T>C	ENSP00000325527.5:n.7571-23T>C
ENST00000559133.5:c.2940-23T>C
NM_000138.4:c.7571-23T>C , LRG_778t1:c.7571-23T>C	NP_000129.3:n.7571-23T>C
NM_000138.5:c.7571-23T>C MANE Select	NP_000129.3:n.7571-23T>C