Canonical Allele Identifier: CA2730865481
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2141277741

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472485G>A , CM000677.2:g.48472485G>A GRCh38
NC_000015.9:g.48764682G>A , CM000677.1:g.48764682G>A GRCh37
NC_000015.8:g.46551974G>A NCBI36
NG_008805.2:g.178304C>T , LRG_778:g.178304C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4336+66C>T ENSP00000453958.2:n.4336+66C>T
ENST00000674301.2:c.4336+66C>T ENSP00000501333.2:n.4336+66C>T
ENST00000683268.1:n.303+66C>T
ENST00000684448.1:n.3010+66C>T
ENST00000316623.10:c.4336+66C>T MANE Select ENSP00000325527.5:n.4336+66C>T
ENST00000316623.9:c.4336+66C>T ENSP00000325527.5:n.4336+66C>T
ENST00000537463.6:c.*99+66C>T ENSP00000440294.2:n.*99+66C>T
NM_000138.4:c.4336+66C>T , LRG_778t1:c.4336+66C>T NP_000129.3:n.4336+66C>T
NM_000138.5:c.4336+66C>T MANE Select NP_000129.3:n.4336+66C>T