Canonical Allele Identifier: CA969560972
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472410C>A , CM000677.2:g.48472410C>A GRCh38
NC_000015.9:g.48764607C>A , CM000677.1:g.48764607C>A GRCh37
NC_000015.8:g.46551899C>A NCBI36
NG_008805.2:g.178379G>T , LRG_778:g.178379G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4336+141G>T ENSP00000453958.2:n.4336+141G>T
ENST00000674301.2:c.4336+141G>T ENSP00000501333.2:n.4336+141G>T
ENST00000683268.1:n.303+141G>T
ENST00000684448.1:n.3010+141G>T
ENST00000316623.10:c.4336+141G>T MANE Select ENSP00000325527.5:n.4336+141G>T
ENST00000316623.9:c.4336+141G>T ENSP00000325527.5:n.4336+141G>T
ENST00000537463.6:c.*99+141G>T ENSP00000440294.2:n.*99+141G>T
NM_000138.4:c.4336+141G>T , LRG_778t1:c.4336+141G>T NP_000129.3:n.4336+141G>T
NM_000138.5:c.4336+141G>T MANE Select NP_000129.3:n.4336+141G>T