Canonical Allele Identifier: CA360758071

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127671227T>G (hg19) ; chr5:g.128335535T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335535T>G , CM000667.2:g.128335535T>G	GRCh38
NC_000005.9:g.127671227T>G , CM000667.1:g.127671227T>G	GRCh37
NC_000005.8:g.127699126T>G	NCBI36
NG_008750.1:g.207509A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.551A>C
ENST00000703785.1:n.632A>C
ENST00000262464.9:c.3767A>C MANE Select	ENSP00000262464.4:p.Gln1256Pro
ENST00000262464.8:c.3767A>C	ENSP00000262464.4:p.Gln1256Pro
ENST00000507835.5:c.317A>C	ENSP00000426839.1:p.Gln106Pro
ENST00000508053.5:c.3767A>C	ENSP00000424571.1:p.Gln1256Pro
ENST00000508989.5:c.3668A>C	ENSP00000425596.1:p.Gln1223Pro
ENST00000619499.4:c.3764A>C	ENSP00000482132.1:p.Gln1255Pro
NM_001999.3:c.3767A>C	NP_001990.2:p.Gln1256Pro
XM_017009228.2:c.3614A>C	XP_016864717.1:p.Gln1205Pro
NM_001999.4:c.3767A>C MANE Select	NP_001990.2:p.Gln1256Pro