Canonical Allele Identifier: CA2804071385
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48486860A>G , CM000677.2:g.48486860A>G GRCh38
NC_000015.9:g.48779057A>G , CM000677.1:g.48779057A>G GRCh37
NC_000015.8:g.46566349A>G NCBI36
NG_008805.2:g.163929T>C , LRG_778:g.163929T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3589+215T>C ENSP00000453958.2:n.3589+215T>C
ENST00000674301.2:c.3589+215T>C ENSP00000501333.2:n.3589+215T>C
ENST00000684448.1:n.2263+215T>C
ENST00000316623.10:c.3589+215T>C MANE Select ENSP00000325527.5:n.3589+215T>C
ENST00000316623.9:c.3589+215T>C ENSP00000325527.5:n.3589+215T>C
ENST00000537463.6:c.637-12210T>C ENSP00000440294.2:n.637-12210T>C
NM_000138.4:c.3589+215T>C , LRG_778t1:c.3589+215T>C NP_000129.3:n.3589+215T>C
NM_000138.5:c.3589+215T>C MANE Select NP_000129.3:n.3589+215T>C