Canonical Allele Identifier: CA2628332577

Gene: FBN1

Linked Data

• gnomAD v4: 15-48434485-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434485A>G , CM000677.2:g.48434485A>G	GRCh38
NC_000015.9:g.48726682A>G , CM000677.1:g.48726682A>G	GRCh37
NC_000015.8:g.46513974A>G	NCBI36
NG_008805.2:g.216304T>C , LRG_778:g.216304T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6616+109T>C	ENSP00000453958.2:n.6616+109T>C
ENST00000674301.2:c.6616+109T>C	ENSP00000501333.2:n.6616+109T>C
ENST00000682170.1:n.225+109T>C
ENST00000316623.10:c.6616+109T>C MANE Select	ENSP00000325527.5:n.6616+109T>C
ENST00000674301.1:c.1615+109T>C	ENSP00000501333.1:n.1615+109T>C
ENST00000316623.9:c.6616+109T>C	ENSP00000325527.5:n.6616+109T>C
ENST00000537463.6:c.*2379+109T>C	ENSP00000440294.2:n.*2379+109T>C
ENST00000559133.5:c.1923+109T>C
NM_000138.4:c.6616+109T>C , LRG_778t1:c.6616+109T>C	NP_000129.3:n.6616+109T>C
NM_000138.5:c.6616+109T>C MANE Select	NP_000129.3:n.6616+109T>C