Canonical Allele Identifier: CA392334702

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48726811C>A (hg19) ; chr15:g.48434614C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434614C>A , CM000677.2:g.48434614C>A	GRCh38
NC_000015.9:g.48726811C>A , CM000677.1:g.48726811C>A	GRCh37
NC_000015.8:g.46514103C>A	NCBI36
NG_008805.2:g.216175G>T , LRG_778:g.216175G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6596G>T	ENSP00000453958.2:p.Gly2199Val
ENST00000674301.2:c.6596G>T	ENSP00000501333.2:p.Gly2199Val
ENST00000682170.1:n.205G>T
ENST00000316623.10:c.6596G>T MANE Select	ENSP00000325527.5:p.Gly2199Val
ENST00000674301.1:c.1595G>T	ENSP00000501333.1:p.Gly532Val
ENST00000316623.9:c.6596G>T	ENSP00000325527.5:p.Gly2199Val
ENST00000537463.6:c.*2359G>T	ENSP00000440294.2:n.*2359G>T
ENST00000559133.5:c.1903G>T
NM_000138.4:c.6596G>T , LRG_778t1:c.6596G>T	NP_000129.3:p.Gly2199Val
NM_000138.5:c.6596G>T MANE Select	NP_000129.3:p.Gly2199Val