Canonical Allele Identifier: CA392334659

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48726803T>C (hg19) ; chr15:g.48434606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434606T>C , CM000677.2:g.48434606T>C	GRCh38
NC_000015.9:g.48726803T>C , CM000677.1:g.48726803T>C	GRCh37
NC_000015.8:g.46514095T>C	NCBI36
NG_008805.2:g.216183A>G , LRG_778:g.216183A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6604A>G	ENSP00000453958.2:p.Met2202Val
ENST00000674301.2:c.6604A>G	ENSP00000501333.2:p.Met2202Val
ENST00000682170.1:n.213A>G
ENST00000316623.10:c.6604A>G MANE Select	ENSP00000325527.5:p.Met2202Val
ENST00000674301.1:c.1603A>G	ENSP00000501333.1:p.Met535Val
ENST00000316623.9:c.6604A>G	ENSP00000325527.5:p.Met2202Val
ENST00000537463.6:c.*2367A>G	ENSP00000440294.2:n.*2367A>G
ENST00000559133.5:c.1911A>G
NM_000138.4:c.6604A>G , LRG_778t1:c.6604A>G	NP_000129.3:p.Met2202Val
NM_000138.5:c.6604A>G MANE Select	NP_000129.3:p.Met2202Val