Canonical Allele Identifier: CA050501
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs375465265

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48410957T>C , CM000677.2:g.48410957T>C GRCh38
NC_000015.9:g.48703154T>C , CM000677.1:g.48703154T>C GRCh37
NC_000015.8:g.46490446T>C NCBI36
NG_008805.2:g.239832A>G , LRG_778:g.239832A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1457A>G ENSP00000453958.2:n.*1457A>G
ENST00000682158.1:n.2030A>G
ENST00000682170.1:n.2830A>G
ENST00000682767.1:n.1946A>G
ENST00000316623.10:c.*33A>G MANE Select ENSP00000325527.5:n.*33A>G
ENST00000316623.9:c.*33A>G ENSP00000325527.5:n.*33A>G
ENST00000559133.5:c.4018A>G
NM_000138.4:c.*33A>G , LRG_778t1:c.*33A>G NP_000129.3:n.*33A>G
NM_000138.5:c.*33A>G MANE Select NP_000129.3:n.*33A>G