Canonical Allele Identifier: CA392330559
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48492502G>C , CM000677.2:g.48492502G>C GRCh38
NC_000015.9:g.48784699G>C , CM000677.1:g.48784699G>C GRCh37
NC_000015.8:g.46571991G>C NCBI36
NG_008805.2:g.158287C>G , LRG_778:g.158287C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2813C>G ENSP00000453958.2:p.Pro938Arg
ENST00000674301.2:c.2813C>G ENSP00000501333.2:p.Pro938Arg
ENST00000684448.1:n.1487C>G
ENST00000316623.10:c.2813C>G MANE Select ENSP00000325527.5:p.Pro938Arg
ENST00000316623.9:c.2813C>G ENSP00000325527.5:p.Pro938Arg
ENST00000537463.6:c.637-17852C>G ENSP00000440294.2:n.637-17852C>G
NM_000138.4:c.2813C>G , LRG_778t1:c.2813C>G NP_000129.3:p.Pro938Arg
NM_000138.5:c.2813C>G MANE Select NP_000129.3:p.Pro938Arg