Canonical Allele Identifier: CA392335716
Gene: FBN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.48789525C>T (hg19) chr15:g.48497328C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48497328C>T , CM000677.2:g.48497328C>T GRCh38
NC_000015.9:g.48789525C>T , CM000677.1:g.48789525C>T GRCh37
NC_000015.8:g.46576817C>T NCBI36
NG_008805.2:g.153461G>A , LRG_778:g.153461G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2231G>A ENSP00000453958.2:p.Gly744Glu
ENST00000674301.2:c.2231G>A ENSP00000501333.2:p.Gly744Glu
ENST00000684448.1:n.905G>A
ENST00000316623.10:c.2231G>A MANE Select ENSP00000325527.5:p.Gly744Glu
ENST00000316623.9:c.2231G>A ENSP00000325527.5:p.Gly744Glu
ENST00000537463.6:c.637-22678G>A ENSP00000440294.2:n.637-22678G>A
NM_000138.4:c.2231G>A , LRG_778t1:c.2231G>A NP_000129.3:p.Gly744Glu
NM_000138.5:c.2231G>A MANE Select NP_000129.3:p.Gly744Glu
Search 100 bp 5'
Search 100 bp 3'