Canonical Allele Identifier: CA969564468

Gene: FBN1

Linked Data

• dbSNP Id: rs2043734643
• gnomAD v3: 15-48508825-G-A
• gnomAD v4: 15-48508825-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48508825G>A , CM000677.2:g.48508825G>A	GRCh38
NC_000015.9:g.48801022G>A , CM000677.1:g.48801022G>A	GRCh37
NC_000015.8:g.46588314G>A	NCBI36
NG_008805.2:g.141964C>T , LRG_778:g.141964C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.1715-121C>T	ENSP00000453958.2:n.1715-121C>T
ENST00000674301.2:c.1715-121C>T	ENSP00000501333.2:n.1715-121C>T
ENST00000684448.1:n.389-121C>T
ENST00000316623.10:c.1715-121C>T MANE Select	ENSP00000325527.5:n.1715-121C>T
ENST00000316623.9:c.1715-121C>T	ENSP00000325527.5:n.1715-121C>T
ENST00000537463.6:c.636+28886C>T	ENSP00000440294.2:n.636+28886C>T
NM_000138.4:c.1715-121C>T , LRG_778t1:c.1715-121C>T	NP_000129.3:n.1715-121C>T
NM_000138.5:c.1715-121C>T MANE Select	NP_000129.3:n.1715-121C>T