Canonical Allele Identifier: CA713393275

Gene: FBN1

Linked Data

• dbSNP Id: rs749780534
• gnomAD v3: 15-48430636-T-C
• gnomAD v4: 15-48430636-T-C
• MyVariant Identifiers: chr15:g.48722833T>C (hg19) ; chr15:g.48430636T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48430636T>C , CM000677.2:g.48430636T>C	GRCh38
NC_000015.9:g.48722833T>C , CM000677.1:g.48722833T>C	GRCh37
NC_000015.8:g.46510125T>C	NCBI36
NG_008805.2:g.220153A>G , LRG_778:g.220153A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6871+35A>G	ENSP00000453958.2:n.6871+35A>G
ENST00000674301.2:c.*322+35A>G	ENSP00000501333.2:n.*322+35A>G
ENST00000682170.1:n.480+35A>G
ENST00000316623.10:c.6871+35A>G MANE Select	ENSP00000325527.5:n.6871+35A>G
ENST00000674301.1:c.1975+35A>G	ENSP00000501333.1:n.1975+35A>G
ENST00000316623.9:c.6871+35A>G	ENSP00000325527.5:n.6871+35A>G
ENST00000559133.5:c.2178+35A>G
ENST00000560720.1:n.158+35A>G
NM_000138.4:c.6871+35A>G , LRG_778t1:c.6871+35A>G	NP_000129.3:n.6871+35A>G
NM_000138.5:c.6871+35A>G MANE Select	NP_000129.3:n.6871+35A>G