Canonical Allele Identifier: CA392338174

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48796027A>C (hg19) ; chr15:g.48503830A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48503830A>C , CM000677.2:g.48503830A>C	GRCh38
NC_000015.9:g.48796027A>C , CM000677.1:g.48796027A>C	GRCh37
NC_000015.8:g.46583319A>C	NCBI36
NG_008805.2:g.146959T>G , LRG_778:g.146959T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.2070T>G	ENSP00000453958.2:p.Tyr690Ter
ENST00000674301.2:c.2070T>G	ENSP00000501333.2:p.Tyr690Ter
ENST00000684448.1:n.744T>G
ENST00000316623.10:c.2070T>G MANE Select	ENSP00000325527.5:p.Tyr690Ter
ENST00000316623.9:c.2070T>G	ENSP00000325527.5:p.Tyr690Ter
ENST00000537463.6:c.637-29180T>G	ENSP00000440294.2:n.637-29180T>G
NM_000138.4:c.2070T>G , LRG_778t1:c.2070T>G	NP_000129.3:p.Tyr690Ter
NM_000138.5:c.2070T>G MANE Select	NP_000129.3:p.Tyr690Ter