Canonical Allele Identifier: CA269557618

Gene: FBN1

Linked Data

• dbSNP Id: rs1031691847
• gnomAD v4: 15-48513644-G-A
• MyVariant Identifiers: chr15:g.48805841G>A (hg19) ; chr15:g.48513644G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48513644G>A , CM000677.2:g.48513644G>A	GRCh38
NC_000015.9:g.48805841G>A , CM000677.1:g.48805841G>A	GRCh37
NC_000015.8:g.46593133G>A	NCBI36
NG_008805.2:g.137145C>T , LRG_778:g.137145C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.1493C>T	ENSP00000453958.2:p.Pro498Leu
ENST00000674301.2:c.1493C>T	ENSP00000501333.2:p.Pro498Leu
ENST00000684448.1:n.167C>T
ENST00000316623.10:c.1493C>T MANE Select	ENSP00000325527.5:p.Pro498Leu
ENST00000316623.9:c.1493C>T	ENSP00000325527.5:p.Pro498Leu
ENST00000537463.6:c.636+24067C>T	ENSP00000440294.2:n.636+24067C>T
NM_000138.4:c.1493C>T , LRG_778t1:c.1493C>T	NP_000129.3:p.Pro498Leu
NM_000138.5:c.1493C>T MANE Select	NP_000129.3:p.Pro498Leu