Canonical Allele Identifier: CA269519971

Gene: FBN1

Linked Data

• dbSNP Id: rs777898950
• MyVariant Identifiers: chr15:g.48714547A>C (hg19) ; chr15:g.48422350A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48422350A>C , CM000677.2:g.48422350A>C	GRCh38
NC_000015.9:g.48714547A>C , CM000677.1:g.48714547A>C	GRCh37
NC_000015.8:g.46501839A>C	NCBI36
NG_008805.2:g.228439T>G , LRG_778:g.228439T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*262-282T>G	ENSP00000453958.2:n.*262-282T>G
ENST00000674301.2:c.*967-282T>G	ENSP00000501333.2:n.*967-282T>G
ENST00000682170.1:n.1635-282T>G
ENST00000682767.1:n.751-282T>G
ENST00000316623.10:c.7454-282T>G MANE Select	ENSP00000325527.5:n.7454-282T>G
ENST00000674301.1:c.2620-282T>G	ENSP00000501333.1:n.2620-282T>G
ENST00000316623.9:c.7454-282T>G	ENSP00000325527.5:n.7454-282T>G
ENST00000559133.5:c.2823-282T>G
NM_000138.4:c.7454-282T>G , LRG_778t1:c.7454-282T>G	NP_000129.3:n.7454-282T>G
NM_000138.5:c.7454-282T>G MANE Select	NP_000129.3:n.7454-282T>G