Canonical Allele Identifier: CA044885
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs762111810

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48513633C>T , CM000677.2:g.48513633C>T GRCh38
NC_000015.9:g.48805830C>T , CM000677.1:g.48805830C>T GRCh37
NC_000015.8:g.46593122C>T NCBI36
NG_008805.2:g.137156G>A , LRG_778:g.137156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1504G>A ENSP00000453958.2:p.Gly502Ser
ENST00000674301.2:c.1504G>A ENSP00000501333.2:p.Gly502Ser
ENST00000684448.1:n.178G>A
ENST00000316623.10:c.1504G>A MANE Select ENSP00000325527.5:p.Gly502Ser
ENST00000316623.9:c.1504G>A ENSP00000325527.5:p.Gly502Ser
ENST00000537463.6:c.636+24078G>A ENSP00000440294.2:n.636+24078G>A
NM_000138.4:c.1504G>A , LRG_778t1:c.1504G>A NP_000129.3:p.Gly502Ser
NM_000138.5:c.1504G>A MANE Select NP_000129.3:p.Gly502Ser