Canonical Allele Identifier: CA713392358
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs1171908920
gnomAD v4: 15-48494364-A-T
MyVariant Identifiers: chr15:g.48786561A>T (hg19) chr15:g.48494364A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48494364A>T , CM000677.2:g.48494364A>T GRCh38
NC_000015.9:g.48786561A>T , CM000677.1:g.48786561A>T GRCh37
NC_000015.8:g.46573853A>T NCBI36
NG_008805.2:g.156425T>A , LRG_778:g.156425T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2678-110T>A ENSP00000453958.2:n.2678-110T>A
ENST00000674301.2:c.2678-110T>A ENSP00000501333.2:n.2678-110T>A
ENST00000684448.1:n.1352-110T>A
ENST00000316623.10:c.2678-110T>A MANE Select ENSP00000325527.5:n.2678-110T>A
ENST00000316623.9:c.2678-110T>A ENSP00000325527.5:n.2678-110T>A
ENST00000537463.6:c.637-19714T>A ENSP00000440294.2:n.637-19714T>A
NM_000138.4:c.2678-110T>A , LRG_778t1:c.2678-110T>A NP_000129.3:n.2678-110T>A
NM_000138.5:c.2678-110T>A MANE Select NP_000129.3:n.2678-110T>A
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