Canonical Allele Identifier: CA2628330024
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425339G>C , CM000677.2:g.48425339G>C GRCh38
NC_000015.9:g.48717536G>C , CM000677.1:g.48717536G>C GRCh37
NC_000015.8:g.46504828G>C NCBI36
NG_008805.2:g.225450C>G , LRG_778:g.225450C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*261+30C>G ENSP00000453958.2:n.*261+30C>G
ENST00000674301.2:c.*966+30C>G ENSP00000501333.2:n.*966+30C>G
ENST00000682170.1:n.1634+30C>G
ENST00000682767.1:n.750+30C>G
ENST00000316623.10:c.7453+30C>G MANE Select ENSP00000325527.5:n.7453+30C>G
ENST00000674301.1:c.2619+30C>G ENSP00000501333.1:n.2619+30C>G
ENST00000316623.9:c.7453+30C>G ENSP00000325527.5:n.7453+30C>G
ENST00000559133.5:c.2822+30C>G
NM_000138.4:c.7453+30C>G , LRG_778t1:c.7453+30C>G NP_000129.3:n.7453+30C>G
NM_000138.5:c.7453+30C>G MANE Select NP_000129.3:n.7453+30C>G