Canonical Allele Identifier: CA16614411

Gene: FBN1

Linked Data

• ClinVar Variation Id: 406371
• ClinVar RCV Id: RCV001181375 ; RCV001193546
• dbSNP Id: rs1060501097
• gnomAD v3: 15-48446718-T-C
• gnomAD v4: 15-48446718-T-C
• MyVariant Identifiers: chr15:g.48738915T>C (hg19) ; chr15:g.48446718T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48446718T>C , CM000677.2:g.48446718T>C	GRCh38
NC_000015.9:g.48738915T>C , CM000677.1:g.48738915T>C	GRCh37
NC_000015.8:g.46526207T>C	NCBI36
NG_008805.2:g.204071A>G , LRG_778:g.204071A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.5776A>G	ENSP00000453958.2:p.Asn1926Asp
ENST00000674301.2:c.5776A>G	ENSP00000501333.2:p.Asn1926Asp
ENST00000684448.1:n.4450A>G
ENST00000316623.10:c.5776A>G MANE Select	ENSP00000325527.5:p.Asn1926Asp
ENST00000674301.1:c.775A>G	ENSP00000501333.1:p.Asn259Asp
ENST00000316623.9:c.5776A>G	ENSP00000325527.5:p.Asn1926Asp
ENST00000537463.6:c.*1539A>G	ENSP00000440294.2:n.*1539A>G
ENST00000559133.5:c.1083A>G
NM_000138.4:c.5776A>G , LRG_778t1:c.5776A>G	NP_000129.3:p.Asn1926Asp
NM_000138.5:c.5776A>G MANE Select	NP_000129.3:p.Asn1926Asp