Canonical Allele Identifier: CA490015248
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043404593
MyVariant Identifiers: chr15:g.48766774G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474577G>A , CM000677.2:g.48474577G>A GRCh38
NC_000015.9:g.48766774G>A , CM000677.1:g.48766774G>A GRCh37
NC_000015.8:g.46554066G>A NCBI36
NG_008805.2:g.176212C>T , LRG_778:g.176212C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4038C>T ENSP00000453958.2:p.Phe1346=
ENST00000674301.2:c.4038C>T ENSP00000501333.2:p.Phe1346=
ENST00000684448.1:n.2712C>T
ENST00000316623.10:c.4038C>T MANE Select ENSP00000325527.5:p.Phe1346=
ENST00000316623.9:c.4038C>T ENSP00000325527.5:p.Phe1346=
ENST00000537463.6:c.710C>T ENSP00000440294.2:p.Ser237Leu
NM_000138.4:c.4038C>T , LRG_778t1:c.4038C>T NP_000129.3:p.Phe1346=
NM_000138.5:c.4038C>T MANE Select NP_000129.3:p.Phe1346=