Canonical Allele Identifier: CA2175518370
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043339833

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468313dup , CM000677.2:g.48468313dup GRCh38
NC_000015.9:g.48760510dup , CM000677.1:g.48760510dup GRCh37
NC_000015.8:g.46547802dup NCBI36
NG_008805.2:g.182476dup , LRG_778:g.182476dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4582+99dup ENSP00000453958.2:n.4582+99dup
ENST00000674301.2:c.4582+99dup ENSP00000501333.2:n.4582+99dup
ENST00000684448.1:n.3256+99dup
ENST00000316623.10:c.4582+99dup MANE Select ENSP00000325527.5:n.4582+99dup
ENST00000316623.9:c.4582+99dup ENSP00000325527.5:n.4582+99dup
ENST00000537463.6:c.*345+99dup ENSP00000440294.2:n.*345+99dup
NM_000138.4:c.4582+99dup , LRG_778t1:c.4582+99dup NP_000129.3:n.4582+99dup
NM_000138.5:c.4582+99dup MANE Select NP_000129.3:n.4582+99dup