Canonical Allele Identifier: CA2175498631
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428541T= , CM000677.2:g.48428541T= GRCh38
NC_000015.9:g.48720738T= , CM000677.1:g.48720738T= GRCh37
NC_000015.8:g.46508030T= NCBI36
NG_008805.2:g.222248A= , LRG_778:g.222248A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6872-70A= ENSP00000453958.2:n.6872-70A=
ENST00000674301.2:c.*323-70A= ENSP00000501333.2:n.*323-70A=
ENST00000682170.1:n.481-70A=
ENST00000682767.1:n.37A=
ENST00000316623.10:c.6872-70A= MANE Select ENSP00000325527.5:n.6872-70A=
ENST00000674301.1:c.1976-70A= ENSP00000501333.1:n.1976-70A=
ENST00000316623.9:c.6872-70A= ENSP00000325527.5:n.6872-70A=
ENST00000559133.5:c.2179-70A=
ENST00000560720.1:n.159-70A=
NM_000138.4:c.6872-70A= , LRG_778t1:c.6872-70A= NP_000129.3:n.6872-70A=
NM_000138.5:c.6872-70A= MANE Select NP_000129.3:n.6872-70A=