Canonical Allele Identifier: CA058584

Gene: FBN1

Linked Data

• dbSNP Id: rs746337953
• ExAC: 15:48717527 C / T
• gnomAD v2: 15-48717527-C-T
• gnomAD v4: 15-48425330-C-T
• MyVariant Identifiers: chr15:g.48717527C>T (hg19) ; chr15:g.48425330C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48425330C>T , CM000677.2:g.48425330C>T	GRCh38
NC_000015.9:g.48717527C>T , CM000677.1:g.48717527C>T	GRCh37
NC_000015.8:g.46504819C>T	NCBI36
NG_008805.2:g.225459G>A , LRG_778:g.225459G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*261+39G>A	ENSP00000453958.2:n.*261+39G>A
ENST00000674301.2:c.*966+39G>A	ENSP00000501333.2:n.*966+39G>A
ENST00000682170.1:n.1634+39G>A
ENST00000682767.1:n.750+39G>A
ENST00000316623.10:c.7453+39G>A MANE Select	ENSP00000325527.5:n.7453+39G>A
ENST00000674301.1:c.2619+39G>A	ENSP00000501333.1:n.2619+39G>A
ENST00000316623.9:c.7453+39G>A	ENSP00000325527.5:n.7453+39G>A
ENST00000559133.5:c.2822+39G>A
NM_000138.4:c.7453+39G>A , LRG_778t1:c.7453+39G>A	NP_000129.3:n.7453+39G>A
NM_000138.5:c.7453+39G>A MANE Select	NP_000129.3:n.7453+39G>A