Canonical Allele Identifier: CA490015303
Gene: FBN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.48766822T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474625T>A , CM000677.2:g.48474625T>A GRCh38
NC_000015.9:g.48766822T>A , CM000677.1:g.48766822T>A GRCh37
NC_000015.8:g.46554114T>A NCBI36
NG_008805.2:g.176164A>T , LRG_778:g.176164A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3990A>T ENSP00000453958.2:p.Ala1330=
ENST00000674301.2:c.3990A>T ENSP00000501333.2:p.Ala1330=
ENST00000684448.1:n.2664A>T
ENST00000316623.10:c.3990A>T MANE Select ENSP00000325527.5:p.Ala1330=
ENST00000316623.9:c.3990A>T ENSP00000325527.5:p.Ala1330=
ENST00000537463.6:c.662A>T ENSP00000440294.2:p.His221Leu
NM_000138.4:c.3990A>T , LRG_778t1:c.3990A>T NP_000129.3:p.Ala1330=
NM_000138.5:c.3990A>T MANE Select NP_000129.3:p.Ala1330=