Canonical Allele Identifier: CA2175539162
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537449G= , CM000677.2:g.48537449G= GRCh38
NC_000015.9:g.48829646G= , CM000677.1:g.48829646G= GRCh37
NC_000015.8:g.46616938G= NCBI36
NG_008805.2:g.113340C= , LRG_778:g.113340C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.736+162C= ENSP00000453958.2:n.736+162C=
ENST00000674301.2:c.736+162C= ENSP00000501333.2:n.736+162C=
ENST00000316623.10:c.736+162C= MANE Select ENSP00000325527.5:n.736+162C=
ENST00000316623.9:c.736+162C= ENSP00000325527.5:n.736+162C=
ENST00000537463.6:c.636+262C= ENSP00000440294.2:n.636+262C=
NM_000138.4:c.736+162C= , LRG_778t1:c.736+162C= NP_000129.3:n.736+162C=
NM_000138.5:c.736+162C= MANE Select NP_000129.3:n.736+162C=