Canonical Allele Identifier: CA2581214117
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48408950A>T , CM000677.2:g.48408950A>T GRCh38
NC_000015.9:g.48701147A>T , CM000677.1:g.48701147A>T GRCh37
NC_000015.8:g.46488439A>T NCBI36
NG_008805.2:g.241839T>A , LRG_778:g.241839T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682170.1:n.4837T>A
ENST00000682767.1:n.3953T>A
ENST00000316623.10:c.*2040T>A MANE Select ENSP00000325527.5:n.*2040T>A
ENST00000316623.9:c.*2040T>A ENSP00000325527.5:n.*2040T>A
NM_000138.4:c.*2040T>A , LRG_778t1:c.*2040T>A NP_000129.3:n.*2040T>A
NM_000138.5:c.*2040T>A MANE Select NP_000129.3:n.*2040T>A