Canonical Allele Identifier: CA2175518549
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468737C= , CM000677.2:g.48468737C= GRCh38
NC_000015.9:g.48760934C= , CM000677.1:g.48760934C= GRCh37
NC_000015.8:g.46548226C= NCBI36
NG_008805.2:g.182052G= , LRG_778:g.182052G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4460-203G= ENSP00000453958.2:n.4460-203G=
ENST00000674301.2:c.4460-203G= ENSP00000501333.2:n.4460-203G=
ENST00000684448.1:n.3134-203G=
ENST00000316623.10:c.4460-203G= MANE Select ENSP00000325527.5:n.4460-203G=
ENST00000316623.9:c.4460-203G= ENSP00000325527.5:n.4460-203G=
ENST00000537463.6:c.*223-203G= ENSP00000440294.2:n.*223-203G=
NM_000138.4:c.4460-203G= , LRG_778t1:c.4460-203G= NP_000129.3:n.4460-203G=
NM_000138.5:c.4460-203G= MANE Select NP_000129.3:n.4460-203G=