Canonical Allele Identifier: CA2628338196
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48612897G>A , CM000677.2:g.48612897G>A GRCh38
NC_000015.9:g.48905094G>A , CM000677.1:g.48905094G>A GRCh37
NC_000015.8:g.46692386G>A NCBI36
NG_008805.2:g.37892C>T , LRG_778:g.37892C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.247+113C>T ENSP00000453958.2:n.247+113C>T
ENST00000674301.2:c.247+113C>T ENSP00000501333.2:n.247+113C>T
ENST00000316623.10:c.247+113C>T MANE Select ENSP00000325527.5:n.247+113C>T
ENST00000316623.9:c.247+113C>T ENSP00000325527.5:n.247+113C>T
ENST00000537463.6:c.247+113C>T ENSP00000440294.2:n.247+113C>T
NM_000138.4:c.247+113C>T , LRG_778t1:c.247+113C>T NP_000129.3:n.247+113C>T
NM_000138.5:c.247+113C>T MANE Select NP_000129.3:n.247+113C>T