Canonical Allele Identifier: CA013848
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 200013
dbSNP Id: rs794728202

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48488403C>A , CM000677.2:g.48488403C>A GRCh38
NC_000015.9:g.48780600C>A , CM000677.1:g.48780600C>A GRCh37
NC_000015.8:g.46567892C>A NCBI36
NG_008805.2:g.162386G>T , LRG_778:g.162386G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3173G>T ENSP00000453958.2:p.Gly1058Val
ENST00000674301.2:c.3173G>T ENSP00000501333.2:p.Gly1058Val
ENST00000684448.1:n.1847G>T
ENST00000316623.10:c.3173G>T MANE Select ENSP00000325527.5:p.Gly1058Val
ENST00000316623.9:c.3173G>T ENSP00000325527.5:p.Gly1058Val
ENST00000537463.6:c.637-13753G>T ENSP00000440294.2:n.637-13753G>T
NM_000138.4:c.3173G>T , LRG_778t1:c.3173G>T NP_000129.3:p.Gly1058Val
NM_000138.5:c.3173G>T MANE Select NP_000129.3:p.Gly1058Val