Canonical Allele Identifier: CA2175539176
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2044022169

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537463dup , CM000677.2:g.48537463dup GRCh38
NC_000015.9:g.48829660dup , CM000677.1:g.48829660dup GRCh37
NC_000015.8:g.46616952dup NCBI36
NG_008805.2:g.113326dup , LRG_778:g.113326dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.736+148dup ENSP00000453958.2:n.736+148dup
ENST00000674301.2:c.736+148dup ENSP00000501333.2:n.736+148dup
ENST00000316623.10:c.736+148dup MANE Select ENSP00000325527.5:n.736+148dup
ENST00000316623.9:c.736+148dup ENSP00000325527.5:n.736+148dup
ENST00000537463.6:c.636+248dup ENSP00000440294.2:n.636+248dup
NM_000138.4:c.736+148dup , LRG_778t1:c.736+148dup NP_000129.3:n.736+148dup
NM_000138.5:c.736+148dup MANE Select NP_000129.3:n.736+148dup