Canonical Allele Identifier: CA392328329
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429319
dbSNP Id: rs1131691317

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48488493T>C , CM000677.2:g.48488493T>C GRCh38
NC_000015.9:g.48780690T>C , CM000677.1:g.48780690T>C GRCh37
NC_000015.8:g.46567982T>C NCBI36
NG_008805.2:g.162296A>G , LRG_778:g.162296A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3083A>G ENSP00000453958.2:p.Asp1028Gly
ENST00000674301.2:c.3083A>G ENSP00000501333.2:p.Asp1028Gly
ENST00000684448.1:n.1757A>G
ENST00000316623.10:c.3083A>G MANE Select ENSP00000325527.5:p.Asp1028Gly
ENST00000316623.9:c.3083A>G ENSP00000325527.5:p.Asp1028Gly
ENST00000537463.6:c.637-13843A>G ENSP00000440294.2:n.637-13843A>G
NM_000138.4:c.3083A>G , LRG_778t1:c.3083A>G NP_000129.3:p.Asp1028Gly
NM_000138.5:c.3083A>G MANE Select NP_000129.3:p.Asp1028Gly