Canonical Allele Identifier: CA2575717218
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48492620T>C , CM000677.2:g.48492620T>C GRCh38
NC_000015.9:g.48784817T>C , CM000677.1:g.48784817T>C GRCh37
NC_000015.8:g.46572109T>C NCBI36
NG_008805.2:g.158169A>G , LRG_778:g.158169A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2729-34A>G ENSP00000453958.2:n.2729-34A>G
ENST00000674301.2:c.2729-34A>G ENSP00000501333.2:n.2729-34A>G
ENST00000684448.1:n.1403-34A>G
ENST00000316623.10:c.2729-34A>G MANE Select ENSP00000325527.5:n.2729-34A>G
ENST00000316623.9:c.2729-34A>G ENSP00000325527.5:n.2729-34A>G
ENST00000537463.6:c.637-17970A>G ENSP00000440294.2:n.637-17970A>G
NM_000138.4:c.2729-34A>G , LRG_778t1:c.2729-34A>G NP_000129.3:n.2729-34A>G
NM_000138.5:c.2729-34A>G MANE Select NP_000129.3:n.2729-34A>G