Canonical Allele Identifier: CA969540674
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2042944267

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421763A>C , CM000677.2:g.48421763A>C GRCh38
NC_000015.9:g.48713960A>C , CM000677.1:g.48713960A>C GRCh37
NC_000015.8:g.46501252A>C NCBI36
NG_008805.2:g.229026T>G , LRG_778:g.229026T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*379-77T>G ENSP00000453958.2:n.*379-77T>G
ENST00000674301.2:c.*1084-77T>G ENSP00000501333.2:n.*1084-77T>G
ENST00000682170.1:n.1752-77T>G
ENST00000682767.1:n.868-77T>G
ENST00000316623.10:c.7571-77T>G MANE Select ENSP00000325527.5:n.7571-77T>G
ENST00000674301.1:c.2737-77T>G ENSP00000501333.1:n.2737-77T>G
ENST00000316623.9:c.7571-77T>G ENSP00000325527.5:n.7571-77T>G
ENST00000559133.5:c.2940-77T>G
NM_000138.4:c.7571-77T>G , LRG_778t1:c.7571-77T>G NP_000129.3:n.7571-77T>G
NM_000138.5:c.7571-77T>G MANE Select NP_000129.3:n.7571-77T>G