Canonical Allele Identifier: CA392335239

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48726895G>T (hg19) ; chr15:g.48434698G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434698G>T , CM000677.2:g.48434698G>T	GRCh38
NC_000015.9:g.48726895G>T , CM000677.1:g.48726895G>T	GRCh37
NC_000015.8:g.46514187G>T	NCBI36
NG_008805.2:g.216091C>A , LRG_778:g.216091C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6512C>A	ENSP00000453958.2:p.Ser2171Tyr
ENST00000674301.2:c.6512C>A	ENSP00000501333.2:p.Ser2171Tyr
ENST00000682170.1:n.121C>A
ENST00000316623.10:c.6512C>A MANE Select	ENSP00000325527.5:p.Ser2171Tyr
ENST00000674301.1:c.1511C>A	ENSP00000501333.1:p.Ser504Tyr
ENST00000316623.9:c.6512C>A	ENSP00000325527.5:p.Ser2171Tyr
ENST00000537463.6:c.*2275C>A	ENSP00000440294.2:n.*2275C>A
ENST00000559133.5:c.1819C>A
NM_000138.4:c.6512C>A , LRG_778t1:c.6512C>A	NP_000129.3:p.Ser2171Tyr
NM_000138.5:c.6512C>A MANE Select	NP_000129.3:p.Ser2171Tyr