Canonical Allele Identifier: CA392333494

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48725128T>G (hg19) ; chr15:g.48432931T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48432931T>G , CM000677.2:g.48432931T>G	GRCh38
NC_000015.9:g.48725128T>G , CM000677.1:g.48725128T>G	GRCh37
NC_000015.8:g.46512420T>G	NCBI36
NG_008805.2:g.217858A>C , LRG_778:g.217858A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6674A>C	ENSP00000453958.2:p.Tyr2225Ser
ENST00000674301.2:c.*125A>C	ENSP00000501333.2:n.*125A>C
ENST00000682170.1:n.283A>C
ENST00000316623.10:c.6674A>C MANE Select	ENSP00000325527.5:p.Tyr2225Ser
ENST00000674301.1:c.1778A>C	ENSP00000501333.1:n.1778A>C
ENST00000316623.9:c.6674A>C	ENSP00000325527.5:p.Tyr2225Ser
ENST00000537463.6:c.*2437A>C	ENSP00000440294.2:n.*2437A>C
ENST00000559133.5:c.1981A>C
NM_000138.4:c.6674A>C , LRG_778t1:c.6674A>C	NP_000129.3:p.Tyr2225Ser
NM_000138.5:c.6674A>C MANE Select	NP_000129.3:p.Tyr2225Ser