Canonical Allele Identifier: CA392322485

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707737G>C (hg19) ; chr15:g.48415540G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415540G>C , CM000677.2:g.48415540G>C	GRCh38
NC_000015.9:g.48707737G>C , CM000677.1:g.48707737G>C	GRCh37
NC_000015.8:g.46495029G>C	NCBI36
NG_008805.2:g.235249C>G , LRG_778:g.235249C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*855C>G	ENSP00000453958.2:n.*855C>G
ENST00000674301.2:c.*1560C>G	ENSP00000501333.2:n.*1560C>G
ENST00000682158.1:n.1428C>G
ENST00000682170.1:n.2228C>G
ENST00000682767.1:n.1344C>G
ENST00000316623.10:c.8047C>G MANE Select	ENSP00000325527.5:p.Gln2683Glu
ENST00000674301.1:c.3213C>G	ENSP00000501333.1:n.3213C>G
ENST00000316623.9:c.8047C>G	ENSP00000325527.5:p.Gln2683Glu
ENST00000559133.5:c.3416C>G
ENST00000561429.1:n.302C>G
NM_000138.4:c.8047C>G , LRG_778t1:c.8047C>G	NP_000129.3:p.Gln2683Glu
NM_000138.5:c.8047C>G MANE Select	NP_000129.3:p.Gln2683Glu