Canonical Allele Identifier: CA052497
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 925008
ClinVar RCV Id: RCV001186742 RCV002497647
dbSNP Id: rs560230585
ExAC: 15:48764756 G / A
gnomAD v2: 15-48764756-G-A
gnomAD v3: 15-48472559-G-A
gnomAD v4: 15-48472559-G-A
MyVariant Identifiers: chr15:g.48764756G>A (hg19) chr15:g.48472559G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472559G>A , CM000677.2:g.48472559G>A GRCh38
NC_000015.9:g.48764756G>A , CM000677.1:g.48764756G>A GRCh37
NC_000015.8:g.46552048G>A NCBI36
NG_008805.2:g.178230C>T , LRG_778:g.178230C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4328C>T ENSP00000453958.2:p.Ala1443Val
ENST00000674301.2:c.4328C>T ENSP00000501333.2:p.Ala1443Val
ENST00000683268.1:n.295C>T
ENST00000684448.1:n.3002C>T
ENST00000316623.10:c.4328C>T MANE Select ENSP00000325527.5:p.Ala1443Val
ENST00000316623.9:c.4328C>T ENSP00000325527.5:p.Ala1443Val
ENST00000537463.6:c.*91C>T ENSP00000440294.2:n.*91C>T
NM_000138.4:c.4328C>T , LRG_778t1:c.4328C>T NP_000129.3:p.Ala1443Val
NM_000138.5:c.4328C>T MANE Select NP_000129.3:p.Ala1443Val
Search 100 bp 5'
Search 100 bp 3'