Canonical Allele Identifier: CA011893
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 42280
ClinVar RCV Id: RCV000035113 RCV001387167
dbSNP Id: rs397515753
MyVariant Identifiers: chr15:g.48812952G>A (hg19) chr15:g.48520755G>A (hg38)
PubMed: PMID:17657824
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48520755G>A , CM000677.2:g.48520755G>A GRCh38
NC_000015.9:g.48812952G>A , CM000677.1:g.48812952G>A GRCh37
NC_000015.8:g.46600244G>A NCBI36
NG_008805.2:g.130034C>T , LRG_778:g.130034C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1051C>T ENSP00000453958.2:p.Gln351Ter
ENST00000674301.2:c.1051C>T ENSP00000501333.2:p.Gln351Ter
ENST00000316623.10:c.1051C>T MANE Select ENSP00000325527.5:p.Gln351Ter
ENST00000316623.9:c.1051C>T ENSP00000325527.5:p.Gln351Ter
ENST00000537463.6:c.636+16956C>T ENSP00000440294.2:n.636+16956C>T
NM_000138.4:c.1051C>T , LRG_778t1:c.1051C>T NP_000129.3:p.Gln351Ter
NM_000138.5:c.1051C>T MANE Select NP_000129.3:p.Gln351Ter
Search 100 bp 5'
Search 100 bp 3'