Canonical Allele Identifier: CA392326077

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48714236T>G (hg19) ; chr15:g.48422039T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48422039T>G , CM000677.2:g.48422039T>G	GRCh38
NC_000015.9:g.48714236T>G , CM000677.1:g.48714236T>G	GRCh37
NC_000015.8:g.46501528T>G	NCBI36
NG_008805.2:g.228750A>C , LRG_778:g.228750A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*291A>C	ENSP00000453958.2:n.*291A>C
ENST00000674301.2:c.*996A>C	ENSP00000501333.2:n.*996A>C
ENST00000682170.1:n.1664A>C
ENST00000682767.1:n.780A>C
ENST00000316623.10:c.7483A>C MANE Select	ENSP00000325527.5:p.Asn2495His
ENST00000674301.1:c.2649A>C	ENSP00000501333.1:n.2649A>C
ENST00000316623.9:c.7483A>C	ENSP00000325527.5:p.Asn2495His
ENST00000559133.5:c.2852A>C
NM_000138.4:c.7483A>C , LRG_778t1:c.7483A>C	NP_000129.3:p.Asn2495His
NM_000138.5:c.7483A>C MANE Select	NP_000129.3:p.Asn2495His