Canonical Allele Identifier: CA2628324371
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2141207766

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48409406T>C , CM000677.2:g.48409406T>C GRCh38
NC_000015.9:g.48701603T>C , CM000677.1:g.48701603T>C GRCh37
NC_000015.8:g.46488895T>C NCBI36
NG_008805.2:g.241383A>G , LRG_778:g.241383A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682170.1:n.4381A>G
ENST00000682767.1:n.3497A>G
ENST00000316623.10:c.*1584A>G MANE Select ENSP00000325527.5:n.*1584A>G
ENST00000316623.9:c.*1584A>G ENSP00000325527.5:n.*1584A>G
NM_000138.4:c.*1584A>G , LRG_778t1:c.*1584A>G NP_000129.3:n.*1584A>G
NM_000138.5:c.*1584A>G MANE Select NP_000129.3:n.*1584A>G