Canonical Allele Identifier: CA2575716798
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48427481G>A , CM000677.2:g.48427481G>A GRCh38
NC_000015.9:g.48719678G>A , CM000677.1:g.48719678G>A GRCh37
NC_000015.8:g.46506970G>A NCBI36
NG_008805.2:g.223308C>T , LRG_778:g.223308C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*12+86C>T ENSP00000453958.2:n.*12+86C>T
ENST00000674301.2:c.*717+86C>T ENSP00000501333.2:n.*717+86C>T
ENST00000682170.1:n.1385+86C>T
ENST00000682767.1:n.501+86C>T
ENST00000316623.10:c.7204+86C>T MANE Select ENSP00000325527.5:n.7204+86C>T
ENST00000674301.1:c.2370+86C>T ENSP00000501333.1:n.2370+86C>T
ENST00000316623.9:c.7204+86C>T ENSP00000325527.5:n.7204+86C>T
ENST00000559133.5:c.2573+86C>T
NM_000138.4:c.7204+86C>T , LRG_778t1:c.7204+86C>T NP_000129.3:n.7204+86C>T
NM_000138.5:c.7204+86C>T MANE Select NP_000129.3:n.7204+86C>T