Canonical Allele Identifier: CA2175518486
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs1284875082

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468575A>C , CM000677.2:g.48468575A>C GRCh38
NC_000015.9:g.48760772A>C , CM000677.1:g.48760772A>C GRCh37
NC_000015.8:g.46548064A>C NCBI36
NG_008805.2:g.182214T>G , LRG_778:g.182214T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4460-41T>G ENSP00000453958.2:n.4460-41T>G
ENST00000674301.2:c.4460-41T>G ENSP00000501333.2:n.4460-41T>G
ENST00000684448.1:n.3134-41T>G
ENST00000316623.10:c.4460-41T>G MANE Select ENSP00000325527.5:n.4460-41T>G
ENST00000316623.9:c.4460-41T>G ENSP00000325527.5:n.4460-41T>G
ENST00000537463.6:c.*223-41T>G ENSP00000440294.2:n.*223-41T>G
NM_000138.4:c.4460-41T>G , LRG_778t1:c.4460-41T>G NP_000129.3:n.4460-41T>G
NM_000138.5:c.4460-41T>G MANE Select NP_000129.3:n.4460-41T>G