Canonical Allele Identifier: CA2175484832
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48409455C= , CM000677.2:g.48409455C= GRCh38
NC_000015.9:g.48701652C= , CM000677.1:g.48701652C= GRCh37
NC_000015.8:g.46488944C= NCBI36
NG_008805.2:g.241334G= , LRG_778:g.241334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682170.1:n.4332G=
ENST00000682767.1:n.3448G=
ENST00000316623.10:c.*1535G= MANE Select ENSP00000325527.5:n.*1535G=
ENST00000316623.9:c.*1535G= ENSP00000325527.5:n.*1535G=
NM_000138.4:c.*1535G= , LRG_778t1:c.*1535G= NP_000129.3:n.*1535G=
NM_000138.5:c.*1535G= MANE Select NP_000129.3:n.*1535G=