Canonical Allele Identifier: CA2175518364

Gene: FBN1

Linked Data

• dbSNP Id: rs2043339738

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48468291T>A , CM000677.2:g.48468291T>A	GRCh38
NC_000015.9:g.48760488T>A , CM000677.1:g.48760488T>A	GRCh37
NC_000015.8:g.46547780T>A	NCBI36
NG_008805.2:g.182498A>T , LRG_778:g.182498A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.4582+121A>T	ENSP00000453958.2:n.4582+121A>T
ENST00000674301.2:c.4582+121A>T	ENSP00000501333.2:n.4582+121A>T
ENST00000684448.1:n.3256+121A>T
ENST00000316623.10:c.4582+121A>T MANE Select	ENSP00000325527.5:n.4582+121A>T
ENST00000316623.9:c.4582+121A>T	ENSP00000325527.5:n.4582+121A>T
ENST00000537463.6:c.*345+121A>T	ENSP00000440294.2:n.*345+121A>T
NM_000138.4:c.4582+121A>T , LRG_778t1:c.4582+121A>T	NP_000129.3:n.4582+121A>T
NM_000138.5:c.4582+121A>T MANE Select	NP_000129.3:n.4582+121A>T