Canonical Allele Identifier: CA490023393

Gene: FBN1

Linked Data

• gnomAD v4: 15-48448886-A-G
• MyVariant Identifiers: chr15:g.48741083A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48448886A>G , CM000677.2:g.48448886A>G	GRCh38
NC_000015.9:g.48741083A>G , CM000677.1:g.48741083A>G	GRCh37
NC_000015.8:g.46528375A>G	NCBI36
NG_008805.2:g.201903T>C , LRG_778:g.201903T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5553T>C	ENSP00000453958.2:p.Asn1851=
ENST00000674301.2:c.5553T>C	ENSP00000501333.2:p.Asn1851=
ENST00000684448.1:n.4227T>C
ENST00000316623.10:c.5553T>C MANE Select	ENSP00000325527.5:p.Asn1851=
ENST00000674301.1:c.552T>C	ENSP00000501333.1:p.Asn184=
ENST00000316623.9:c.5553T>C	ENSP00000325527.5:p.Asn1851=
ENST00000537463.6:c.*1316T>C	ENSP00000440294.2:n.*1316T>C
ENST00000559133.5:c.860T>C
NM_000138.4:c.5553T>C , LRG_778t1:c.5553T>C	NP_000129.3:p.Asn1851=
NM_000138.5:c.5553T>C MANE Select	NP_000129.3:p.Asn1851=