Canonical Allele Identifier: CA392332599
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48430758G>C , CM000677.2:g.48430758G>C GRCh38
NC_000015.9:g.48722955G>C , CM000677.1:g.48722955G>C GRCh37
NC_000015.8:g.46510247G>C NCBI36
NG_008805.2:g.220031C>G , LRG_778:g.220031C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6784C>G ENSP00000453958.2:p.Gln2262Glu
ENST00000674301.2:c.*235C>G ENSP00000501333.2:n.*235C>G
ENST00000682170.1:n.393C>G
ENST00000316623.10:c.6784C>G MANE Select ENSP00000325527.5:p.Gln2262Glu
ENST00000674301.1:c.1888C>G ENSP00000501333.1:n.1888C>G
ENST00000316623.9:c.6784C>G ENSP00000325527.5:p.Gln2262Glu
ENST00000559133.5:c.2091C>G
ENST00000560720.1:n.71C>G
NM_000138.4:c.6784C>G , LRG_778t1:c.6784C>G NP_000129.3:p.Gln2262Glu
NM_000138.5:c.6784C>G MANE Select NP_000129.3:p.Gln2262Glu