Canonical Allele Identifier: CA446310609

Gene: FBN2

Linked Data

• dbSNP Id: rs778088321
• gnomAD v3: 5-128338049-C-T
• gnomAD v4: 5-128338049-C-T
• MyVariant Identifiers: chr5:g.127673741C>T (hg19) ; chr5:g.128338049C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338049C>T , CM000667.2:g.128338049C>T	GRCh38
NC_000005.9:g.127673741C>T , CM000667.1:g.127673741C>T	GRCh37
NC_000005.8:g.127701640C>T	NCBI36
NG_008750.1:g.204995G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.330G>A
ENST00000703785.1:n.411G>A
ENST00000262464.9:c.3546G>A MANE Select	ENSP00000262464.4:p.Gln1182=
ENST00000262464.8:c.3546G>A	ENSP00000262464.4:p.Gln1182=
ENST00000507835.5:c.96G>A	ENSP00000426839.1:p.Gln32=
ENST00000508053.5:c.3546G>A	ENSP00000424571.1:p.Gln1182=
ENST00000508989.5:c.3447G>A	ENSP00000425596.1:p.Gln1149=
ENST00000619499.4:c.3543G>A	ENSP00000482132.1:p.Gln1181=
NM_001999.3:c.3546G>A	NP_001990.2:p.Gln1182=
XM_017009228.2:c.3393G>A	XP_016864717.1:p.Gln1131=
NM_001999.4:c.3546G>A MANE Select	NP_001990.2:p.Gln1182=