Canonical Allele Identifier: CA392333170

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48725065T>C (hg19) ; chr15:g.48432868T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48432868T>C , CM000677.2:g.48432868T>C	GRCh38
NC_000015.9:g.48725065T>C , CM000677.1:g.48725065T>C	GRCh37
NC_000015.8:g.46512357T>C	NCBI36
NG_008805.2:g.217921A>G , LRG_778:g.217921A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6737A>G	ENSP00000453958.2:p.Lys2246Arg
ENST00000674301.2:c.*188A>G	ENSP00000501333.2:n.*188A>G
ENST00000682170.1:n.346A>G
ENST00000316623.10:c.6737A>G MANE Select	ENSP00000325527.5:p.Lys2246Arg
ENST00000674301.1:c.1841A>G	ENSP00000501333.1:n.1841A>G
ENST00000316623.9:c.6737A>G	ENSP00000325527.5:p.Lys2246Arg
ENST00000537463.6:c.*2500A>G	ENSP00000440294.2:n.*2500A>G
ENST00000559133.5:c.2044A>G
ENST00000560720.1:n.24A>G
NM_000138.4:c.6737A>G , LRG_778t1:c.6737A>G	NP_000129.3:p.Lys2246Arg
NM_000138.5:c.6737A>G MANE Select	NP_000129.3:p.Lys2246Arg