Canonical Allele Identifier: CA490021620

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48734000G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441803G>C , CM000677.2:g.48441803G>C	GRCh38
NC_000015.9:g.48734000G>C , CM000677.1:g.48734000G>C	GRCh37
NC_000015.8:g.46521292G>C	NCBI36
NG_008805.2:g.208986C>G , LRG_778:g.208986C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6081C>G	ENSP00000453958.2:p.Gly2027=
ENST00000674301.2:c.6081C>G	ENSP00000501333.2:p.Gly2027=
ENST00000316623.10:c.6081C>G MANE Select	ENSP00000325527.5:p.Gly2027=
ENST00000674301.1:c.1080C>G	ENSP00000501333.1:p.Gly360=
ENST00000316623.9:c.6081C>G	ENSP00000325527.5:p.Gly2027=
ENST00000537463.6:c.*1844C>G	ENSP00000440294.2:n.*1844C>G
ENST00000559133.5:c.1388C>G
ENST00000560820.1:n.201C>G
NM_000138.4:c.6081C>G , LRG_778t1:c.6081C>G	NP_000129.3:p.Gly2027=
NM_000138.5:c.6081C>G MANE Select	NP_000129.3:p.Gly2027=