Canonical Allele Identifier: CA2175539164
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537451G= , CM000677.2:g.48537451G= GRCh38
NC_000015.9:g.48829648G= , CM000677.1:g.48829648G= GRCh37
NC_000015.8:g.46616940G= NCBI36
NG_008805.2:g.113338C= , LRG_778:g.113338C=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.736+160C= ENSP00000453958.2:n.736+160C=
ENST00000674301.2:c.736+160C= ENSP00000501333.2:n.736+160C=
ENST00000316623.10:c.736+160C= MANE Select ENSP00000325527.5:n.736+160C=
ENST00000316623.9:c.736+160C= ENSP00000325527.5:n.736+160C=
ENST00000537463.6:c.636+260C= ENSP00000440294.2:n.636+260C=
NM_000138.4:c.736+160C= , LRG_778t1:c.736+160C= NP_000129.3:n.736+160C=
NM_000138.5:c.736+160C= MANE Select NP_000129.3:n.736+160C=