Canonical Allele Identifier: CA269552564
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs1014486285
MyVariant Identifiers: chr15:g.48760835A>T (hg19) chr15:g.48468638A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468638A>T , CM000677.2:g.48468638A>T GRCh38
NC_000015.9:g.48760835A>T , CM000677.1:g.48760835A>T GRCh37
NC_000015.8:g.46548127A>T NCBI36
NG_008805.2:g.182151T>A , LRG_778:g.182151T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4460-104T>A ENSP00000453958.2:n.4460-104T>A
ENST00000674301.2:c.4460-104T>A ENSP00000501333.2:n.4460-104T>A
ENST00000684448.1:n.3134-104T>A
ENST00000316623.10:c.4460-104T>A MANE Select ENSP00000325527.5:n.4460-104T>A
ENST00000316623.9:c.4460-104T>A ENSP00000325527.5:n.4460-104T>A
ENST00000537463.6:c.*223-104T>A ENSP00000440294.2:n.*223-104T>A
NM_000138.4:c.4460-104T>A , LRG_778t1:c.4460-104T>A NP_000129.3:n.4460-104T>A
NM_000138.5:c.4460-104T>A MANE Select NP_000129.3:n.4460-104T>A
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