Canonical Allele Identifier: CA016275

Gene: FBN1

Linked Data

• ClinVar Variation Id: 200076
• ClinVar RCV Id: RCV000181559 ; RCV000245533 ; RCV000525187 ; RCV000663852 ; RCV002509285 ; RCV000769629
• dbSNP Id: rs763091520
• MyVariant Identifiers: chr15:g.48730109G>A (hg19) ; chr15:g.48437912G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48437912G>A , CM000677.2:g.48437912G>A	GRCh38
NC_000015.9:g.48730109G>A , CM000677.1:g.48730109G>A	GRCh37
NC_000015.8:g.46517401G>A	NCBI36
NG_008805.2:g.212877C>T , LRG_778:g.212877C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6169C>T	ENSP00000453958.2:p.Arg2057Ter
ENST00000674301.2:c.6169C>T	ENSP00000501333.2:p.Arg2057Ter
ENST00000316623.10:c.6169C>T MANE Select	ENSP00000325527.5:p.Arg2057Ter
ENST00000674301.1:c.1168C>T	ENSP00000501333.1:p.Arg390Ter
ENST00000316623.9:c.6169C>T	ENSP00000325527.5:p.Arg2057Ter
ENST00000537463.6:c.*1932C>T	ENSP00000440294.2:n.*1932C>T
ENST00000559133.5:c.1476C>T
ENST00000560820.1:n.289C>T
NM_000138.4:c.6169C>T , LRG_778t1:c.6169C>T	NP_000129.3:p.Arg2057Ter
NM_000138.5:c.6169C>T MANE Select	NP_000129.3:p.Arg2057Ter