Canonical Allele Identifier: CA2175463262
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421556A= , CM000677.2:g.48421556A= GRCh38
NC_000015.9:g.48713753A= , CM000677.1:g.48713753A= GRCh37
NC_000015.8:g.46501045A= NCBI36
NG_008805.2:g.229233T= , LRG_778:g.229233T=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*507+2T= ENSP00000453958.2:n.*507+2T=
ENST00000674301.2:c.*1212+2T= ENSP00000501333.2:n.*1212+2T=
ENST00000682170.1:n.1880+2T=
ENST00000682767.1:n.996+2T=
ENST00000316623.10:c.7699+2T= MANE Select ENSP00000325527.5:n.7699+2T=
ENST00000674301.1:c.2865+2T= ENSP00000501333.1:n.2865+2T=
ENST00000316623.9:c.7699+2T= ENSP00000325527.5:n.7699+2T=
ENST00000559133.5:c.3068+2T=
NM_000138.4:c.7699+2T= , LRG_778t1:c.7699+2T= NP_000129.3:n.7699+2T=
NM_000138.5:c.7699+2T= MANE Select NP_000129.3:n.7699+2T=