Canonical Allele Identifier: CA2175463931
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2042944106

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421749A>G , CM000677.2:g.48421749A>G GRCh38
NC_000015.9:g.48713946A>G , CM000677.1:g.48713946A>G GRCh37
NC_000015.8:g.46501238A>G NCBI36
NG_008805.2:g.229040T>C , LRG_778:g.229040T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*379-63T>C ENSP00000453958.2:n.*379-63T>C
ENST00000674301.2:c.*1084-63T>C ENSP00000501333.2:n.*1084-63T>C
ENST00000682170.1:n.1752-63T>C
ENST00000682767.1:n.868-63T>C
ENST00000316623.10:c.7571-63T>C MANE Select ENSP00000325527.5:n.7571-63T>C
ENST00000674301.1:c.2737-63T>C ENSP00000501333.1:n.2737-63T>C
ENST00000316623.9:c.7571-63T>C ENSP00000325527.5:n.7571-63T>C
ENST00000559133.5:c.2940-63T>C
NM_000138.4:c.7571-63T>C , LRG_778t1:c.7571-63T>C NP_000129.3:n.7571-63T>C
NM_000138.5:c.7571-63T>C MANE Select NP_000129.3:n.7571-63T>C