Canonical Allele Identifier: CA2175498678
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428551C= , CM000677.2:g.48428551C= GRCh38
NC_000015.9:g.48720748C= , CM000677.1:g.48720748C= GRCh37
NC_000015.8:g.46508040C= NCBI36
NG_008805.2:g.222238G= , LRG_778:g.222238G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6872-80G= ENSP00000453958.2:n.6872-80G=
ENST00000674301.2:c.*323-80G= ENSP00000501333.2:n.*323-80G=
ENST00000682170.1:n.481-80G=
ENST00000682767.1:n.27G=
ENST00000316623.10:c.6872-80G= MANE Select ENSP00000325527.5:n.6872-80G=
ENST00000674301.1:c.1976-80G= ENSP00000501333.1:n.1976-80G=
ENST00000316623.9:c.6872-80G= ENSP00000325527.5:n.6872-80G=
ENST00000559133.5:c.2179-80G=
ENST00000560720.1:n.159-80G=
NM_000138.4:c.6872-80G= , LRG_778t1:c.6872-80G= NP_000129.3:n.6872-80G=
NM_000138.5:c.6872-80G= MANE Select NP_000129.3:n.6872-80G=