Canonical Allele Identifier: CA2628332806
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48434723A>G , CM000677.2:g.48434723A>G GRCh38
NC_000015.9:g.48726920A>G , CM000677.1:g.48726920A>G GRCh37
NC_000015.8:g.46514212A>G NCBI36
NG_008805.2:g.216066T>C , LRG_778:g.216066T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6497-10T>C ENSP00000453958.2:n.6497-10T>C
ENST00000674301.2:c.6497-10T>C ENSP00000501333.2:n.6497-10T>C
ENST00000682170.1:n.106-10T>C
ENST00000316623.10:c.6497-10T>C MANE Select ENSP00000325527.5:n.6497-10T>C
ENST00000674301.1:c.1496-10T>C ENSP00000501333.1:n.1496-10T>C
ENST00000316623.9:c.6497-10T>C ENSP00000325527.5:n.6497-10T>C
ENST00000537463.6:c.*2260-10T>C ENSP00000440294.2:n.*2260-10T>C
ENST00000559133.5:c.1804-10T>C
NM_000138.4:c.6497-10T>C , LRG_778t1:c.6497-10T>C NP_000129.3:n.6497-10T>C
NM_000138.5:c.6497-10T>C MANE Select NP_000129.3:n.6497-10T>C