Canonical Allele Identifier: CA269518333
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs897442902

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48408543G>C , CM000677.2:g.48408543G>C GRCh38
NC_000015.9:g.48700740G>C , CM000677.1:g.48700740G>C GRCh37
NC_000015.8:g.46488032G>C NCBI36
NG_008805.2:g.242246C>G , LRG_778:g.242246C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682170.1:n.5244C>G
ENST00000682767.1:n.4360C>G
ENST00000316623.10:c.*2447C>G MANE Select ENSP00000325527.5:n.*2447C>G
ENST00000316623.9:c.*2447C>G ENSP00000325527.5:n.*2447C>G
NM_000138.4:c.*2447C>G , LRG_778t1:c.*2447C>G NP_000129.3:n.*2447C>G
NM_000138.5:c.*2447C>G MANE Select NP_000129.3:n.*2447C>G