Canonical Allele Identifier: CA392329347
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48489960C>G , CM000677.2:g.48489960C>G GRCh38
NC_000015.9:g.48782157C>G , CM000677.1:g.48782157C>G GRCh37
NC_000015.8:g.46569449C>G NCBI36
NG_008805.2:g.160829G>C , LRG_778:g.160829G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.2973G>C ENSP00000453958.2:p.Glu991Asp
ENST00000674301.2:c.2973G>C ENSP00000501333.2:p.Glu991Asp
ENST00000684448.1:n.1647G>C
ENST00000316623.10:c.2973G>C MANE Select ENSP00000325527.5:p.Glu991Asp
ENST00000316623.9:c.2973G>C ENSP00000325527.5:p.Glu991Asp
ENST00000537463.6:c.637-15310G>C ENSP00000440294.2:n.637-15310G>C
NM_000138.4:c.2973G>C , LRG_778t1:c.2973G>C NP_000129.3:p.Glu991Asp
NM_000138.5:c.2973G>C MANE Select NP_000129.3:p.Glu991Asp