Canonical Allele Identifier: CA392320048
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 549212
ClinVar RCV Id: RCV000663699
dbSNP Id: rs1555397653
MyVariant Identifiers: chr15:g.48766479A>G (hg19) chr15:g.48474282A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474282A>G , CM000677.2:g.48474282A>G GRCh38
NC_000015.9:g.48766479A>G , CM000677.1:g.48766479A>G GRCh37
NC_000015.8:g.46553771A>G NCBI36
NG_008805.2:g.176507T>C , LRG_778:g.176507T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4183T>C ENSP00000453958.2:p.Tyr1395His
ENST00000674301.2:c.4183T>C ENSP00000501333.2:p.Tyr1395His
ENST00000684448.1:n.2857T>C
ENST00000316623.10:c.4183T>C MANE Select ENSP00000325527.5:p.Tyr1395His
ENST00000316623.9:c.4183T>C ENSP00000325527.5:p.Tyr1395His
ENST00000537463.6:c.855T>C ENSP00000440294.2:p.Asp285=
NM_000138.4:c.4183T>C , LRG_778t1:c.4183T>C NP_000129.3:p.Tyr1395His
NM_000138.5:c.4183T>C MANE Select NP_000129.3:p.Tyr1395His
Search 100 bp 5'
Search 100 bp 3'