Canonical Allele Identifier: CA969542806
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043001903

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428686A>T , CM000677.2:g.48428686A>T GRCh38
NC_000015.9:g.48720883A>T , CM000677.1:g.48720883A>T GRCh37
NC_000015.8:g.46508175A>T NCBI36
NG_008805.2:g.222103T>A , LRG_778:g.222103T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6872-215T>A ENSP00000453958.2:n.6872-215T>A
ENST00000674301.2:c.*323-215T>A ENSP00000501333.2:n.*323-215T>A
ENST00000682170.1:n.481-215T>A
ENST00000316623.10:c.6872-215T>A MANE Select ENSP00000325527.5:n.6872-215T>A
ENST00000674301.1:c.1976-215T>A ENSP00000501333.1:n.1976-215T>A
ENST00000316623.9:c.6872-215T>A ENSP00000325527.5:n.6872-215T>A
ENST00000559133.5:c.2179-215T>A
ENST00000560720.1:n.159-215T>A
NM_000138.4:c.6872-215T>A , LRG_778t1:c.6872-215T>A NP_000129.3:n.6872-215T>A
NM_000138.5:c.6872-215T>A MANE Select NP_000129.3:n.6872-215T>A