Canonical Allele Identifier: CA2175508489
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441647G= , CM000677.2:g.48441647G= GRCh38
NC_000015.9:g.48733844G= , CM000677.1:g.48733844G= GRCh37
NC_000015.8:g.46521136G= NCBI36
NG_008805.2:g.209142C= , LRG_778:g.209142C=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6163+74C= ENSP00000453958.2:n.6163+74C=
ENST00000674301.2:c.6163+74C= ENSP00000501333.2:n.6163+74C=
ENST00000316623.10:c.6163+74C= MANE Select ENSP00000325527.5:n.6163+74C=
ENST00000674301.1:c.1162+74C= ENSP00000501333.1:n.1162+74C=
ENST00000316623.9:c.6163+74C= ENSP00000325527.5:n.6163+74C=
ENST00000537463.6:c.*1926+74C= ENSP00000440294.2:n.*1926+74C=
ENST00000559133.5:c.1470+74C=
ENST00000560820.1:n.283+74C=
NM_000138.4:c.6163+74C= , LRG_778t1:c.6163+74C= NP_000129.3:n.6163+74C=
NM_000138.5:c.6163+74C= MANE Select NP_000129.3:n.6163+74C=