Canonical Allele Identifier: CA2175502279
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48430668T= , CM000677.2:g.48430668T= GRCh38
NC_000015.9:g.48722865T= , CM000677.1:g.48722865T= GRCh37
NC_000015.8:g.46510157T= NCBI36
NG_008805.2:g.220121A= , LRG_778:g.220121A=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6871+3A= ENSP00000453958.2:n.6871+3A=
ENST00000674301.2:c.*322+3A= ENSP00000501333.2:n.*322+3A=
ENST00000682170.1:n.480+3A=
ENST00000316623.10:c.6871+3A= MANE Select ENSP00000325527.5:n.6871+3A=
ENST00000674301.1:c.1975+3A= ENSP00000501333.1:n.1975+3A=
ENST00000316623.9:c.6871+3A= ENSP00000325527.5:n.6871+3A=
ENST00000559133.5:c.2178+3A=
ENST00000560720.1:n.158+3A=
NM_000138.4:c.6871+3A= , LRG_778t1:c.6871+3A= NP_000129.3:n.6871+3A=
NM_000138.5:c.6871+3A= MANE Select NP_000129.3:n.6871+3A=