Canonical Allele Identifier: CA2175518119
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043334396
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48467786T>C , CM000677.2:g.48467786T>C GRCh38
NC_000015.9:g.48759983T>C , CM000677.1:g.48759983T>C GRCh37
NC_000015.8:g.46547275T>C NCBI36
NG_008805.2:g.183003A>G , LRG_778:g.183003A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4747+152A>G ENSP00000453958.2:n.4747+152A>G
ENST00000674301.2:c.4747+152A>G ENSP00000501333.2:n.4747+152A>G
ENST00000684448.1:n.3421+152A>G
ENST00000316623.10:c.4747+152A>G MANE Select ENSP00000325527.5:n.4747+152A>G
ENST00000316623.9:c.4747+152A>G ENSP00000325527.5:n.4747+152A>G
ENST00000537463.6:c.*510+152A>G ENSP00000440294.2:n.*510+152A>G
ENST00000559133.5:c.54+152A>G
NM_000138.4:c.4747+152A>G , LRG_778t1:c.4747+152A>G NP_000129.3:n.4747+152A>G
NM_000138.5:c.4747+152A>G MANE Select NP_000129.3:n.4747+152A>G
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