Canonical Allele Identifier: CA713395800

Gene: FBN1

Linked Data

• dbSNP Id: rs1182717287
• gnomAD v3: 15-48434385-G-T
• gnomAD v4: 15-48434385-G-T
• MyVariant Identifiers: chr15:g.48726582G>T (hg19) ; chr15:g.48434385G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434385G>T , CM000677.2:g.48434385G>T	GRCh38
NC_000015.9:g.48726582G>T , CM000677.1:g.48726582G>T	GRCh37
NC_000015.8:g.46513874G>T	NCBI36
NG_008805.2:g.216404C>A , LRG_778:g.216404C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6616+209C>A	ENSP00000453958.2:n.6616+209C>A
ENST00000674301.2:c.6617-173C>A	ENSP00000501333.2:n.6617-173C>A
ENST00000682170.1:n.225+209C>A
ENST00000316623.10:c.6616+209C>A MANE Select	ENSP00000325527.5:n.6616+209C>A
ENST00000674301.1:c.1616-173C>A	ENSP00000501333.1:n.1616-173C>A
ENST00000316623.9:c.6616+209C>A	ENSP00000325527.5:n.6616+209C>A
ENST00000537463.6:c.*2379+209C>A	ENSP00000440294.2:n.*2379+209C>A
ENST00000559133.5:c.1923+209C>A
NM_000138.4:c.6616+209C>A , LRG_778t1:c.6616+209C>A	NP_000129.3:n.6616+209C>A
NM_000138.5:c.6616+209C>A MANE Select	NP_000129.3:n.6616+209C>A