Canonical Allele Identifier: CA360755306

Gene: FBN2

Linked Data

• gnomAD v4: 5-128333006-A-C
• MyVariant Identifiers: chr5:g.127668698A>C (hg19) ; chr5:g.128333006A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128333006A>C , CM000667.2:g.128333006A>C	GRCh38
NC_000005.9:g.127668698A>C , CM000667.1:g.127668698A>C	GRCh37
NC_000005.8:g.127696597A>C	NCBI36
NG_008750.1:g.210038T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.912T>G
ENST00000703785.1:n.993T>G
ENST00000262464.9:c.4128T>G MANE Select	ENSP00000262464.4:p.His1376Gln
ENST00000262464.8:c.4128T>G	ENSP00000262464.4:p.His1376Gln
ENST00000507835.5:c.678T>G	ENSP00000426839.1:p.His226Gln
ENST00000508053.5:c.4128T>G	ENSP00000424571.1:p.His1376Gln
ENST00000508989.5:c.4029T>G	ENSP00000425596.1:p.His1343Gln
ENST00000619499.4:c.4125T>G	ENSP00000482132.1:p.His1375Gln
NM_001999.3:c.4128T>G	NP_001990.2:p.His1376Gln
XM_017009228.2:c.3975T>G	XP_016864717.1:p.His1325Gln
NM_001999.4:c.4128T>G MANE Select	NP_001990.2:p.His1376Gln