Canonical Allele Identifier: CA2175485382
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48410042C= , CM000677.2:g.48410042C= GRCh38
NC_000015.9:g.48702239C= , CM000677.1:g.48702239C= GRCh37
NC_000015.8:g.46489531C= NCBI36
NG_008805.2:g.240747G= , LRG_778:g.240747G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682170.1:n.3745G=
ENST00000682767.1:n.2861G=
ENST00000316623.10:c.*948G= MANE Select ENSP00000325527.5:n.*948G=
ENST00000316623.9:c.*948G= ENSP00000325527.5:n.*948G=
NM_000138.4:c.*948G= , LRG_778t1:c.*948G= NP_000129.3:n.*948G=
NM_000138.5:c.*948G= MANE Select NP_000129.3:n.*948G=