Canonical Allele Identifier: CA360759456

Gene: FBN2

Linked Data

• gnomAD v4: 5-128338085-C-A
• MyVariant Identifiers: chr5:g.127673777C>A (hg19) ; chr5:g.128338085C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338085C>A , CM000667.2:g.128338085C>A	GRCh38
NC_000005.9:g.127673777C>A , CM000667.1:g.127673777C>A	GRCh37
NC_000005.8:g.127701676C>A	NCBI36
NG_008750.1:g.204959G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.294G>T
ENST00000703785.1:n.375G>T
ENST00000262464.9:c.3510G>T MANE Select	ENSP00000262464.4:p.Arg1170Ser
ENST00000262464.8:c.3510G>T	ENSP00000262464.4:p.Arg1170Ser
ENST00000507835.5:c.60G>T	ENSP00000426839.1:p.Arg20Ser
ENST00000508053.5:c.3510G>T	ENSP00000424571.1:p.Arg1170Ser
ENST00000508989.5:c.3411G>T	ENSP00000425596.1:p.Arg1137Ser
ENST00000619499.4:c.3507G>T	ENSP00000482132.1:p.Arg1169Ser
NM_001999.3:c.3510G>T	NP_001990.2:p.Arg1170Ser
XM_017009228.2:c.3357G>T	XP_016864717.1:p.Arg1119Ser
NM_001999.4:c.3510G>T MANE Select	NP_001990.2:p.Arg1170Ser