Canonical Allele Identifier: CA713401160

Gene: FBN1

Linked Data

• dbSNP Id: rs1019459140
• MyVariant Identifiers: chr15:g.48733901C>A (hg19) ; chr15:g.48441704C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441704C>A , CM000677.2:g.48441704C>A	GRCh38
NC_000015.9:g.48733901C>A , CM000677.1:g.48733901C>A	GRCh37
NC_000015.8:g.46521193C>A	NCBI36
NG_008805.2:g.209085G>T , LRG_778:g.209085G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6163+17G>T	ENSP00000453958.2:n.6163+17G>T
ENST00000674301.2:c.6163+17G>T	ENSP00000501333.2:n.6163+17G>T
ENST00000316623.10:c.6163+17G>T MANE Select	ENSP00000325527.5:n.6163+17G>T
ENST00000674301.1:c.1162+17G>T	ENSP00000501333.1:n.1162+17G>T
ENST00000316623.9:c.6163+17G>T	ENSP00000325527.5:n.6163+17G>T
ENST00000537463.6:c.*1926+17G>T	ENSP00000440294.2:n.*1926+17G>T
ENST00000559133.5:c.1470+17G>T
ENST00000560820.1:n.283+17G>T
NM_000138.4:c.6163+17G>T , LRG_778t1:c.6163+17G>T	NP_000129.3:n.6163+17G>T
NM_000138.5:c.6163+17G>T MANE Select	NP_000129.3:n.6163+17G>T