Canonical Allele Identifier: CA014371
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 200021
dbSNP Id: rs794728207

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485472T>C , CM000677.2:g.48485472T>C GRCh38
NC_000015.9:g.48777669T>C , CM000677.1:g.48777669T>C GRCh37
NC_000015.8:g.46564961T>C NCBI36
NG_008805.2:g.165317A>G , LRG_778:g.165317A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3614A>G ENSP00000453958.2:p.Asn1205Ser
ENST00000674301.2:c.3614A>G ENSP00000501333.2:p.Asn1205Ser
ENST00000684448.1:n.2288A>G
ENST00000316623.10:c.3614A>G MANE Select ENSP00000325527.5:p.Asn1205Ser
ENST00000316623.9:c.3614A>G ENSP00000325527.5:p.Asn1205Ser
ENST00000537463.6:c.637-10822A>G ENSP00000440294.2:n.637-10822A>G
NM_000138.4:c.3614A>G , LRG_778t1:c.3614A>G NP_000129.3:p.Asn1205Ser
NM_000138.5:c.3614A>G MANE Select NP_000129.3:p.Asn1205Ser