Canonical Allele Identifier: CA16619944
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 418200
ClinVar RCV Id: RCV000487361 RCV002245990
dbSNP Id: rs1064793118
MyVariant Identifiers: chr15:g.48729235C>T (hg19) chr15:g.48437038C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48437038C>T , CM000677.2:g.48437038C>T GRCh38
NC_000015.9:g.48729235C>T , CM000677.1:g.48729235C>T GRCh37
NC_000015.8:g.46516527C>T NCBI36
NG_008805.2:g.213751G>A , LRG_778:g.213751G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6419G>A ENSP00000453958.2:p.Gly2140Glu
ENST00000674301.2:c.6419G>A ENSP00000501333.2:p.Gly2140Glu
ENST00000682170.1:n.28G>A
ENST00000316623.10:c.6419G>A MANE Select ENSP00000325527.5:p.Gly2140Glu
ENST00000674301.1:c.1418G>A ENSP00000501333.1:p.Gly473Glu
ENST00000316623.9:c.6419G>A ENSP00000325527.5:p.Gly2140Glu
ENST00000537463.6:c.*2182G>A ENSP00000440294.2:n.*2182G>A
ENST00000559133.5:c.1726G>A
NM_000138.4:c.6419G>A , LRG_778t1:c.6419G>A NP_000129.3:p.Gly2140Glu
NM_000138.5:c.6419G>A MANE Select NP_000129.3:p.Gly2140Glu
Search 100 bp 5'
Search 100 bp 3'