Canonical Allele Identifier: CA2628329561
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421809C>A , CM000677.2:g.48421809C>A GRCh38
NC_000015.9:g.48714006C>A , CM000677.1:g.48714006C>A GRCh37
NC_000015.8:g.46501298C>A NCBI36
NG_008805.2:g.228980G>T , LRG_778:g.228980G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*379-123G>T ENSP00000453958.2:n.*379-123G>T
ENST00000674301.2:c.*1084-123G>T ENSP00000501333.2:n.*1084-123G>T
ENST00000682170.1:n.1752-123G>T
ENST00000682767.1:n.868-123G>T
ENST00000316623.10:c.7571-123G>T MANE Select ENSP00000325527.5:n.7571-123G>T
ENST00000674301.1:c.2737-123G>T ENSP00000501333.1:n.2737-123G>T
ENST00000316623.9:c.7571-123G>T ENSP00000325527.5:n.7571-123G>T
ENST00000559133.5:c.2940-123G>T
NM_000138.4:c.7571-123G>T , LRG_778t1:c.7571-123G>T NP_000129.3:n.7571-123G>T
NM_000138.5:c.7571-123G>T MANE Select NP_000129.3:n.7571-123G>T