Canonical Allele Identifier: CA490015321
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071017
ClinVar RCV Id: RCV004014519
dbSNP Id: rs2043405375
COSMIC: COSM962388
MyVariant Identifiers: chr15:g.48766840A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474643A>G , CM000677.2:g.48474643A>G GRCh38
NC_000015.9:g.48766840A>G , CM000677.1:g.48766840A>G GRCh37
NC_000015.8:g.46554132A>G NCBI36
NG_008805.2:g.176146T>C , LRG_778:g.176146T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3972T>C ENSP00000453958.2:p.Asn1324=
ENST00000674301.2:c.3972T>C ENSP00000501333.2:p.Asn1324=
ENST00000684448.1:n.2646T>C
ENST00000316623.10:c.3972T>C MANE Select ENSP00000325527.5:p.Asn1324=
ENST00000316623.9:c.3972T>C ENSP00000325527.5:p.Asn1324=
ENST00000537463.6:c.644T>C ENSP00000440294.2:p.Met215Thr
NM_000138.4:c.3972T>C , LRG_778t1:c.3972T>C NP_000129.3:p.Asn1324=
NM_000138.5:c.3972T>C MANE Select NP_000129.3:p.Asn1324=