Canonical Allele Identifier: CA2175537590
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48520736T= , CM000677.2:g.48520736T= GRCh38
NC_000015.9:g.48812933T= , CM000677.1:g.48812933T= GRCh37
NC_000015.8:g.46600225T= NCBI36
NG_008805.2:g.130053A= , LRG_778:g.130053A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1070A= ENSP00000453958.2:p.Gln357=
ENST00000674301.2:c.1070A= ENSP00000501333.2:p.Gln357=
ENST00000316623.10:c.1070A= MANE Select ENSP00000325527.5:p.Gln357=
ENST00000316623.9:c.1070A= ENSP00000325527.5:p.Gln357=
ENST00000537463.6:c.636+16975A= ENSP00000440294.2:n.636+16975A=
NM_000138.4:c.1070A= , LRG_778t1:c.1070A= NP_000129.3:p.Gln357=
NM_000138.5:c.1070A= MANE Select NP_000129.3:p.Gln357=