Canonical Allele Identifier: CA2628334272
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441634G>C , CM000677.2:g.48441634G>C GRCh38
NC_000015.9:g.48733831G>C , CM000677.1:g.48733831G>C GRCh37
NC_000015.8:g.46521123G>C NCBI36
NG_008805.2:g.209155C>G , LRG_778:g.209155C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6163+87C>G ENSP00000453958.2:n.6163+87C>G
ENST00000674301.2:c.6163+87C>G ENSP00000501333.2:n.6163+87C>G
ENST00000316623.10:c.6163+87C>G MANE Select ENSP00000325527.5:n.6163+87C>G
ENST00000674301.1:c.1162+87C>G ENSP00000501333.1:n.1162+87C>G
ENST00000316623.9:c.6163+87C>G ENSP00000325527.5:n.6163+87C>G
ENST00000537463.6:c.*1926+87C>G ENSP00000440294.2:n.*1926+87C>G
ENST00000559133.5:c.1470+87C>G
ENST00000560820.1:n.283+87C>G
NM_000138.4:c.6163+87C>G , LRG_778t1:c.6163+87C>G NP_000129.3:n.6163+87C>G
NM_000138.5:c.6163+87C>G MANE Select NP_000129.3:n.6163+87C>G