Canonical Allele Identifier: CA2175508466
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441630C= , CM000677.2:g.48441630C= GRCh38
NC_000015.9:g.48733827C= , CM000677.1:g.48733827C= GRCh37
NC_000015.8:g.46521119C= NCBI36
NG_008805.2:g.209159G= , LRG_778:g.209159G=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6163+91G= ENSP00000453958.2:n.6163+91G=
ENST00000674301.2:c.6163+91G= ENSP00000501333.2:n.6163+91G=
ENST00000316623.10:c.6163+91G= MANE Select ENSP00000325527.5:n.6163+91G=
ENST00000674301.1:c.1162+91G= ENSP00000501333.1:n.1162+91G=
ENST00000316623.9:c.6163+91G= ENSP00000325527.5:n.6163+91G=
ENST00000537463.6:c.*1926+91G= ENSP00000440294.2:n.*1926+91G=
ENST00000559133.5:c.1470+91G=
ENST00000560820.1:n.283+91G=
NM_000138.4:c.6163+91G= , LRG_778t1:c.6163+91G= NP_000129.3:n.6163+91G=
NM_000138.5:c.6163+91G= MANE Select NP_000129.3:n.6163+91G=