Canonical Allele Identifier: CA969550010
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48444468C>A , CM000677.2:g.48444468C>A GRCh38
NC_000015.9:g.48736665C>A , CM000677.1:g.48736665C>A GRCh37
NC_000015.8:g.46523957C>A NCBI36
NG_008805.2:g.206321G>T , LRG_778:g.206321G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6037+73G>T ENSP00000453958.2:n.6037+73G>T
ENST00000674301.2:c.6037+73G>T ENSP00000501333.2:n.6037+73G>T
ENST00000684448.1:n.4784G>T
ENST00000316623.10:c.6037+73G>T MANE Select ENSP00000325527.5:n.6037+73G>T
ENST00000674301.1:c.1036+73G>T ENSP00000501333.1:n.1036+73G>T
ENST00000316623.9:c.6037+73G>T ENSP00000325527.5:n.6037+73G>T
ENST00000537463.6:c.*1800+73G>T ENSP00000440294.2:n.*1800+73G>T
ENST00000559133.5:c.1344+73G>T
ENST00000560820.1:n.157+73G>T
NM_000138.4:c.6037+73G>T , LRG_778t1:c.6037+73G>T NP_000129.3:n.6037+73G>T
NM_000138.5:c.6037+73G>T MANE Select NP_000129.3:n.6037+73G>T