Canonical Allele Identifier: CA490027502
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 918744
dbSNP Id: rs2043341420
MyVariant Identifiers: chr15:g.48760688G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468491G>A , CM000677.2:g.48468491G>A GRCh38
NC_000015.9:g.48760688G>A , CM000677.1:g.48760688G>A GRCh37
NC_000015.8:g.46547980G>A NCBI36
NG_008805.2:g.182298C>T , LRG_778:g.182298C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4503C>T ENSP00000453958.2:p.Asn1501=
ENST00000674301.2:c.4503C>T ENSP00000501333.2:p.Asn1501=
ENST00000684448.1:n.3177C>T
ENST00000316623.10:c.4503C>T MANE Select ENSP00000325527.5:p.Asn1501=
ENST00000316623.9:c.4503C>T ENSP00000325527.5:p.Asn1501=
ENST00000537463.6:c.*266C>T ENSP00000440294.2:n.*266C>T
NM_000138.4:c.4503C>T , LRG_778t1:c.4503C>T NP_000129.3:p.Asn1501=
NM_000138.5:c.4503C>T MANE Select NP_000129.3:p.Asn1501=