Canonical Allele Identifier: CA2628336108
Gene: FBN1 HGNC NCBI

Linked Data

gnomAD v4: 15-48509982-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48509982A>G , CM000677.2:g.48509982A>G GRCh38
NC_000015.9:g.48802179A>G , CM000677.1:g.48802179A>G GRCh37
NC_000015.8:g.46589471A>G NCBI36
NG_008805.2:g.140807T>C , LRG_778:g.140807T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.1714+62T>C ENSP00000453958.2:n.1714+62T>C
ENST00000674301.2:c.1714+62T>C ENSP00000501333.2:n.1714+62T>C
ENST00000684448.1:n.388+62T>C
ENST00000316623.10:c.1714+62T>C MANE Select ENSP00000325527.5:n.1714+62T>C
ENST00000316623.9:c.1714+62T>C ENSP00000325527.5:n.1714+62T>C
ENST00000537463.6:c.636+27729T>C ENSP00000440294.2:n.636+27729T>C
NM_000138.4:c.1714+62T>C , LRG_778t1:c.1714+62T>C NP_000129.3:n.1714+62T>C
NM_000138.5:c.1714+62T>C MANE Select NP_000129.3:n.1714+62T>C
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