Canonical Allele Identifier: CA2628333354
Gene: FBN1 HGNC NCBI

Linked Data

gnomAD v4: 15-48437222-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48437222A>G , CM000677.2:g.48437222A>G GRCh38
NC_000015.9:g.48729419A>G , CM000677.1:g.48729419A>G GRCh37
NC_000015.8:g.46516711A>G NCBI36
NG_008805.2:g.213567T>C , LRG_778:g.213567T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6379+100T>C ENSP00000453958.2:n.6379+100T>C
ENST00000674301.2:c.6379+100T>C ENSP00000501333.2:n.6379+100T>C
ENST00000316623.10:c.6379+100T>C MANE Select ENSP00000325527.5:n.6379+100T>C
ENST00000674301.1:c.1378+100T>C ENSP00000501333.1:n.1378+100T>C
ENST00000316623.9:c.6379+100T>C ENSP00000325527.5:n.6379+100T>C
ENST00000537463.6:c.*2142+100T>C ENSP00000440294.2:n.*2142+100T>C
ENST00000559133.5:c.1686+100T>C
NM_000138.4:c.6379+100T>C , LRG_778t1:c.6379+100T>C NP_000129.3:n.6379+100T>C
NM_000138.5:c.6379+100T>C MANE Select NP_000129.3:n.6379+100T>C
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