Canonical Allele Identifier: CA2628334578
Gene: FBN1 HGNC NCBI

Linked Data

gnomAD v4: 15-48474801-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474801C>A , CM000677.2:g.48474801C>A GRCh38
NC_000015.9:g.48766998C>A , CM000677.1:g.48766998C>A GRCh37
NC_000015.8:g.46554290C>A NCBI36
NG_008805.2:g.175988G>T , LRG_778:g.175988G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3965-151G>T ENSP00000453958.2:n.3965-151G>T
ENST00000674301.2:c.3965-151G>T ENSP00000501333.2:n.3965-151G>T
ENST00000684448.1:n.2639-151G>T
ENST00000316623.10:c.3965-151G>T MANE Select ENSP00000325527.5:n.3965-151G>T
ENST00000316623.9:c.3965-151G>T ENSP00000325527.5:n.3965-151G>T
ENST00000537463.6:c.637-151G>T ENSP00000440294.2:n.637-151G>T
NM_000138.4:c.3965-151G>T , LRG_778t1:c.3965-151G>T NP_000129.3:n.3965-151G>T
NM_000138.5:c.3965-151G>T MANE Select NP_000129.3:n.3965-151G>T
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