Canonical Allele Identifier: CA392340038

Gene: FBN1

Linked Data

• ClinVar Variation Id: 2951024
• ClinVar RCV Id: RCV003802286 ; RCV004006074
• dbSNP Id: rs2043150977
• gnomAD v4: 15-48445429-T-C
• MyVariant Identifiers: chr15:g.48737626T>C (hg19) ; chr15:g.48445429T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445429T>C , CM000677.2:g.48445429T>C	GRCh38
NC_000015.9:g.48737626T>C , CM000677.1:g.48737626T>C	GRCh37
NC_000015.8:g.46524918T>C	NCBI36
NG_008805.2:g.205360A>G , LRG_778:g.205360A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5864A>G	ENSP00000453958.2:p.Gln1955Arg
ENST00000674301.2:c.5864A>G	ENSP00000501333.2:p.Gln1955Arg
ENST00000684448.1:n.4538A>G
ENST00000316623.10:c.5864A>G MANE Select	ENSP00000325527.5:p.Gln1955Arg
ENST00000674301.1:c.863A>G	ENSP00000501333.1:p.Gln288Arg
ENST00000316623.9:c.5864A>G	ENSP00000325527.5:p.Gln1955Arg
ENST00000537463.6:c.*1627A>G	ENSP00000440294.2:n.*1627A>G
ENST00000559133.5:c.1171A>G
NM_000138.4:c.5864A>G , LRG_778t1:c.5864A>G	NP_000129.3:p.Gln1955Arg
NM_000138.5:c.5864A>G MANE Select	NP_000129.3:p.Gln1955Arg