Canonical Allele Identifier: CA490015283
Gene: FBN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.48766801A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474604A>T , CM000677.2:g.48474604A>T GRCh38
NC_000015.9:g.48766801A>T , CM000677.1:g.48766801A>T GRCh37
NC_000015.8:g.46554093A>T NCBI36
NG_008805.2:g.176185T>A , LRG_778:g.176185T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4011T>A ENSP00000453958.2:p.Ala1337=
ENST00000674301.2:c.4011T>A ENSP00000501333.2:p.Ala1337=
ENST00000684448.1:n.2685T>A
ENST00000316623.10:c.4011T>A MANE Select ENSP00000325527.5:p.Ala1337=
ENST00000316623.9:c.4011T>A ENSP00000325527.5:p.Ala1337=
ENST00000537463.6:c.683T>A ENSP00000440294.2:p.Leu228Gln
NM_000138.4:c.4011T>A , LRG_778t1:c.4011T>A NP_000129.3:p.Ala1337=
NM_000138.5:c.4011T>A MANE Select NP_000129.3:p.Ala1337=