Canonical Allele Identifier: CA360759342

Gene: FBN2

Linked Data

• COSMIC: COSM4489876 ; COSM4489877
• MyVariant Identifiers: chr5:g.127673743G>A (hg19) ; chr5:g.128338051G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338051G>A , CM000667.2:g.128338051G>A	GRCh38
NC_000005.9:g.127673743G>A , CM000667.1:g.127673743G>A	GRCh37
NC_000005.8:g.127701642G>A	NCBI36
NG_008750.1:g.204993C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.328C>T
ENST00000703785.1:n.409C>T
ENST00000262464.9:c.3544C>T MANE Select	ENSP00000262464.4:p.Gln1182Ter
ENST00000262464.8:c.3544C>T	ENSP00000262464.4:p.Gln1182Ter
ENST00000507835.5:c.94C>T	ENSP00000426839.1:p.Gln32Ter
ENST00000508053.5:c.3544C>T	ENSP00000424571.1:p.Gln1182Ter
ENST00000508989.5:c.3445C>T	ENSP00000425596.1:p.Gln1149Ter
ENST00000619499.4:c.3541C>T	ENSP00000482132.1:p.Gln1181Ter
NM_001999.3:c.3544C>T	NP_001990.2:p.Gln1182Ter
XM_017009228.2:c.3391C>T	XP_016864717.1:p.Gln1131Ter
NM_001999.4:c.3544C>T MANE Select	NP_001990.2:p.Gln1182Ter