Canonical Allele Identifier: CA269526960
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs953598372
gnomAD v3: 15-48485217-A-T
gnomAD v4: 15-48485217-A-T
MyVariant Identifiers: chr15:g.48777414A>T (hg19) chr15:g.48485217A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485217A>T , CM000677.2:g.48485217A>T GRCh38
NC_000015.9:g.48777414A>T , CM000677.1:g.48777414A>T GRCh37
NC_000015.8:g.46564706A>T NCBI36
NG_008805.2:g.165572T>A , LRG_778:g.165572T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3712+157T>A ENSP00000453958.2:n.3712+157T>A
ENST00000674301.2:c.3712+157T>A ENSP00000501333.2:n.3712+157T>A
ENST00000684448.1:n.2386+157T>A
ENST00000316623.10:c.3712+157T>A MANE Select ENSP00000325527.5:n.3712+157T>A
ENST00000316623.9:c.3712+157T>A ENSP00000325527.5:n.3712+157T>A
ENST00000537463.6:c.637-10567T>A ENSP00000440294.2:n.637-10567T>A
NM_000138.4:c.3712+157T>A , LRG_778t1:c.3712+157T>A NP_000129.3:n.3712+157T>A
NM_000138.5:c.3712+157T>A MANE Select NP_000129.3:n.3712+157T>A
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