Canonical Allele Identifier: CA269518559
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs200718684
gnomAD v2: 15-48702921-A-G
gnomAD v3: 15-48410724-A-G
gnomAD v4: 15-48410724-A-G
MyVariant Identifiers: chr15:g.48702921A>G (hg19) chr15:g.48410724A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48410724A>G , CM000677.2:g.48410724A>G GRCh38
NC_000015.9:g.48702921A>G , CM000677.1:g.48702921A>G GRCh37
NC_000015.8:g.46490213A>G NCBI36
NG_008805.2:g.240065T>C , LRG_778:g.240065T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1690T>C ENSP00000453958.2:n.*1690T>C
ENST00000682158.1:n.2263T>C
ENST00000682170.1:n.3063T>C
ENST00000682767.1:n.2179T>C
ENST00000316623.10:c.*266T>C MANE Select ENSP00000325527.5:n.*266T>C
ENST00000316623.9:c.*266T>C ENSP00000325527.5:n.*266T>C
ENST00000559133.5:c.4251T>C
NM_000138.4:c.*266T>C , LRG_778t1:c.*266T>C NP_000129.3:n.*266T>C
NM_000138.5:c.*266T>C MANE Select NP_000129.3:n.*266T>C
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