Canonical Allele Identifier: CA392342361

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48741064T>C (hg19) ; chr15:g.48448867T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48448867T>C , CM000677.2:g.48448867T>C	GRCh38
NC_000015.9:g.48741064T>C , CM000677.1:g.48741064T>C	GRCh37
NC_000015.8:g.46528356T>C	NCBI36
NG_008805.2:g.201922A>G , LRG_778:g.201922A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5572A>G	ENSP00000453958.2:p.Asn1858Asp
ENST00000674301.2:c.5572A>G	ENSP00000501333.2:p.Asn1858Asp
ENST00000684448.1:n.4246A>G
ENST00000316623.10:c.5572A>G MANE Select	ENSP00000325527.5:p.Asn1858Asp
ENST00000674301.1:c.571A>G	ENSP00000501333.1:p.Asn191Asp
ENST00000316623.9:c.5572A>G	ENSP00000325527.5:p.Asn1858Asp
ENST00000537463.6:c.*1335A>G	ENSP00000440294.2:n.*1335A>G
ENST00000559133.5:c.879A>G
NM_000138.4:c.5572A>G , LRG_778t1:c.5572A>G	NP_000129.3:p.Asn1858Asp
NM_000138.5:c.5572A>G MANE Select	NP_000129.3:p.Asn1858Asp