Canonical Allele Identifier: CA490027436
Gene: FBN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.48760646A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468449A>T , CM000677.2:g.48468449A>T GRCh38
NC_000015.9:g.48760646A>T , CM000677.1:g.48760646A>T GRCh37
NC_000015.8:g.46547938A>T NCBI36
NG_008805.2:g.182340T>A , LRG_778:g.182340T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4545T>A ENSP00000453958.2:p.Pro1515=
ENST00000674301.2:c.4545T>A ENSP00000501333.2:p.Pro1515=
ENST00000684448.1:n.3219T>A
ENST00000316623.10:c.4545T>A MANE Select ENSP00000325527.5:p.Pro1515=
ENST00000316623.9:c.4545T>A ENSP00000325527.5:p.Pro1515=
ENST00000537463.6:c.*308T>A ENSP00000440294.2:n.*308T>A
NM_000138.4:c.4545T>A , LRG_778t1:c.4545T>A NP_000129.3:p.Pro1515=
NM_000138.5:c.4545T>A MANE Select NP_000129.3:p.Pro1515=