Canonical Allele Identifier: CA360757982

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127671189T>G (hg19) ; chr5:g.128335497T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335497T>G , CM000667.2:g.128335497T>G	GRCh38
NC_000005.9:g.127671189T>G , CM000667.1:g.127671189T>G	GRCh37
NC_000005.8:g.127699088T>G	NCBI36
NG_008750.1:g.207547A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.589A>C
ENST00000703785.1:n.670A>C
ENST00000262464.9:c.3805A>C MANE Select	ENSP00000262464.4:p.Ser1269Arg
ENST00000262464.8:c.3805A>C	ENSP00000262464.4:p.Ser1269Arg
ENST00000507835.5:c.355A>C	ENSP00000426839.1:p.Ser119Arg
ENST00000508053.5:c.3805A>C	ENSP00000424571.1:p.Ser1269Arg
ENST00000508989.5:c.3706A>C	ENSP00000425596.1:p.Ser1236Arg
ENST00000619499.4:c.3802A>C	ENSP00000482132.1:p.Ser1268Arg
NM_001999.3:c.3805A>C	NP_001990.2:p.Ser1269Arg
XM_017009228.2:c.3652A>C	XP_016864717.1:p.Ser1218Arg
NM_001999.4:c.3805A>C MANE Select	NP_001990.2:p.Ser1269Arg