Canonical Allele Identifier: CA392341267

Gene: FBN1

Linked Data

• ClinVar Variation Id: 939149
• ClinVar RCV Id: RCV001208494 ; RCV002246019
• dbSNP Id: rs1555400064
• MyVariant Identifiers: chr15:g.48802333C>T (hg19) ; chr15:g.48510136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48510136C>T , CM000677.2:g.48510136C>T	GRCh38
NC_000015.9:g.48802333C>T , CM000677.1:g.48802333C>T	GRCh37
NC_000015.8:g.46589625C>T	NCBI36
NG_008805.2:g.140653G>A , LRG_778:g.140653G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.1622G>A	ENSP00000453958.2:p.Cys541Tyr
ENST00000674301.2:c.1622G>A	ENSP00000501333.2:p.Cys541Tyr
ENST00000684448.1:n.296G>A
ENST00000316623.10:c.1622G>A MANE Select	ENSP00000325527.5:p.Cys541Tyr
ENST00000316623.9:c.1622G>A	ENSP00000325527.5:p.Cys541Tyr
ENST00000537463.6:c.636+27575G>A	ENSP00000440294.2:n.636+27575G>A
NM_000138.4:c.1622G>A , LRG_778t1:c.1622G>A	NP_000129.3:p.Cys541Tyr
NM_000138.5:c.1622G>A MANE Select	NP_000129.3:p.Cys541Tyr