Canonical Allele Identifier: CA2175484089
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2042836149

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48408546A>G , CM000677.2:g.48408546A>G GRCh38
NC_000015.9:g.48700743A>G , CM000677.1:g.48700743A>G GRCh37
NC_000015.8:g.46488035A>G NCBI36
NG_008805.2:g.242243T>C , LRG_778:g.242243T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682170.1:n.5241T>C
ENST00000682767.1:n.4357T>C
ENST00000316623.10:c.*2444T>C MANE Select ENSP00000325527.5:n.*2444T>C
ENST00000316623.9:c.*2444T>C ENSP00000325527.5:n.*2444T>C
NM_000138.4:c.*2444T>C , LRG_778t1:c.*2444T>C NP_000129.3:n.*2444T>C
NM_000138.5:c.*2444T>C MANE Select NP_000129.3:n.*2444T>C