Canonical Allele Identifier: CA490118792
Gene: FBN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.48703250T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411053T>C , CM000677.2:g.48411053T>C GRCh38
NC_000015.9:g.48703250T>C , CM000677.1:g.48703250T>C GRCh37
NC_000015.8:g.46490542T>C NCBI36
NG_008805.2:g.239736A>G , LRG_778:g.239736A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1361A>G ENSP00000453958.2:n.*1361A>G
ENST00000682158.1:n.1934A>G
ENST00000682170.1:n.2734A>G
ENST00000682767.1:n.1850A>G
ENST00000316623.10:c.8553A>G MANE Select ENSP00000325527.5:p.Lys2851=
ENST00000316623.9:c.8553A>G ENSP00000325527.5:p.Lys2851=
ENST00000559133.5:c.3922A>G
NM_000138.4:c.8553A>G , LRG_778t1:c.8553A>G NP_000129.3:p.Lys2851=
NM_000138.5:c.8553A>G MANE Select NP_000129.3:p.Lys2851=