Canonical Allele Identifier: CA2628334264
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441625G>A , CM000677.2:g.48441625G>A GRCh38
NC_000015.9:g.48733822G>A , CM000677.1:g.48733822G>A GRCh37
NC_000015.8:g.46521114G>A NCBI36
NG_008805.2:g.209164C>T , LRG_778:g.209164C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6163+96C>T ENSP00000453958.2:n.6163+96C>T
ENST00000674301.2:c.6163+96C>T ENSP00000501333.2:n.6163+96C>T
ENST00000316623.10:c.6163+96C>T MANE Select ENSP00000325527.5:n.6163+96C>T
ENST00000674301.1:c.1162+96C>T ENSP00000501333.1:n.1162+96C>T
ENST00000316623.9:c.6163+96C>T ENSP00000325527.5:n.6163+96C>T
ENST00000537463.6:c.*1926+96C>T ENSP00000440294.2:n.*1926+96C>T
ENST00000559133.5:c.1470+96C>T
ENST00000560820.1:n.283+96C>T
NM_000138.4:c.6163+96C>T , LRG_778t1:c.6163+96C>T NP_000129.3:n.6163+96C>T
NM_000138.5:c.6163+96C>T MANE Select NP_000129.3:n.6163+96C>T