Canonical Allele Identifier: CA392340078
Gene: FBN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.48737645T>A (hg19) chr15:g.48445448T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445448T>A , CM000677.2:g.48445448T>A GRCh38
NC_000015.9:g.48737645T>A , CM000677.1:g.48737645T>A GRCh37
NC_000015.8:g.46524937T>A NCBI36
NG_008805.2:g.205341A>T , LRG_778:g.205341A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5845A>T ENSP00000453958.2:p.Asn1949Tyr
ENST00000674301.2:c.5845A>T ENSP00000501333.2:p.Asn1949Tyr
ENST00000684448.1:n.4519A>T
ENST00000316623.10:c.5845A>T MANE Select ENSP00000325527.5:p.Asn1949Tyr
ENST00000674301.1:c.844A>T ENSP00000501333.1:p.Asn282Tyr
ENST00000316623.9:c.5845A>T ENSP00000325527.5:p.Asn1949Tyr
ENST00000537463.6:c.*1608A>T ENSP00000440294.2:n.*1608A>T
ENST00000559133.5:c.1152A>T
NM_000138.4:c.5845A>T , LRG_778t1:c.5845A>T NP_000129.3:p.Asn1949Tyr
NM_000138.5:c.5845A>T MANE Select NP_000129.3:p.Asn1949Tyr
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