Canonical Allele Identifier: CA017540
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 42439
ClinVar RCV Id: RCV000035284 RCV000181626 RCV000280634 RCV000284299 RCV000338124 RCV000397502 RCV000372736 RCV000400824 RCV001213083
dbSNP Id: rs145105768
ExAC: 15:48704921 C / T
gnomAD v2: 15-48704921-C-T
gnomAD v3: 15-48412724-C-T
gnomAD v4: 15-48412724-C-T
MyVariant Identifiers: chr15:g.48704921C>T (hg19) chr15:g.48412724C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412724C>T , CM000677.2:g.48412724C>T GRCh38
NC_000015.9:g.48704921C>T , CM000677.1:g.48704921C>T GRCh37
NC_000015.8:g.46492213C>T NCBI36
NG_008805.2:g.238065G>A , LRG_778:g.238065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*879G>A ENSP00000453958.2:n.*879G>A
ENST00000674301.2:c.*1584G>A ENSP00000501333.2:n.*1584G>A
ENST00000682158.1:n.1452G>A
ENST00000682170.1:n.2252G>A
ENST00000682767.1:n.1368G>A
ENST00000316623.10:c.8071G>A MANE Select ENSP00000325527.5:p.Gly2691Ser
ENST00000674301.1:c.3237G>A ENSP00000501333.1:n.3237G>A
ENST00000316623.9:c.8071G>A ENSP00000325527.5:p.Gly2691Ser
ENST00000559133.5:c.3440G>A
ENST00000561429.1:n.326G>A
NM_000138.4:c.8071G>A , LRG_778t1:c.8071G>A NP_000129.3:p.Gly2691Ser
NM_000138.5:c.8071G>A MANE Select NP_000129.3:p.Gly2691Ser
Search 100 bp 5'
Search 100 bp 3'