Canonical Allele Identifier: CA2628324429
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48409580A>G , CM000677.2:g.48409580A>G GRCh38
NC_000015.9:g.48701777A>G , CM000677.1:g.48701777A>G GRCh37
NC_000015.8:g.46489069A>G NCBI36
NG_008805.2:g.241209T>C , LRG_778:g.241209T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682170.1:n.4207T>C
ENST00000682767.1:n.3323T>C
ENST00000316623.10:c.*1410T>C MANE Select ENSP00000325527.5:n.*1410T>C
ENST00000316623.9:c.*1410T>C ENSP00000325527.5:n.*1410T>C
NM_000138.4:c.*1410T>C , LRG_778t1:c.*1410T>C NP_000129.3:n.*1410T>C
NM_000138.5:c.*1410T>C MANE Select NP_000129.3:n.*1410T>C