Canonical Allele Identifier: CA2175495688
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043403488

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474443T>A , CM000677.2:g.48474443T>A GRCh38
NC_000015.9:g.48766640T>A , CM000677.1:g.48766640T>A GRCh37
NC_000015.8:g.46553932T>A NCBI36
NG_008805.2:g.176346A>T , LRG_778:g.176346A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4088-66A>T ENSP00000453958.2:n.4088-66A>T
ENST00000674301.2:c.4088-66A>T ENSP00000501333.2:n.4088-66A>T
ENST00000684448.1:n.2762-66A>T
ENST00000316623.10:c.4088-66A>T MANE Select ENSP00000325527.5:n.4088-66A>T
ENST00000316623.9:c.4088-66A>T ENSP00000325527.5:n.4088-66A>T
ENST00000537463.6:c.760-66A>T ENSP00000440294.2:n.760-66A>T
NM_000138.4:c.4088-66A>T , LRG_778t1:c.4088-66A>T NP_000129.3:n.4088-66A>T
NM_000138.5:c.4088-66A>T MANE Select NP_000129.3:n.4088-66A>T