Canonical Allele Identifier: CA360759276

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127673724C>G (hg19) ; chr5:g.128338032C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338032C>G , CM000667.2:g.128338032C>G	GRCh38
NC_000005.9:g.127673724C>G , CM000667.1:g.127673724C>G	GRCh37
NC_000005.8:g.127701623C>G	NCBI36
NG_008750.1:g.205012G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.347G>C
ENST00000703785.1:n.428G>C
ENST00000262464.9:c.3563G>C MANE Select	ENSP00000262464.4:p.Gly1188Ala
ENST00000262464.8:c.3563G>C	ENSP00000262464.4:p.Gly1188Ala
ENST00000507835.5:c.113G>C	ENSP00000426839.1:p.Gly38Ala
ENST00000508053.5:c.3563G>C	ENSP00000424571.1:p.Gly1188Ala
ENST00000508989.5:c.3464G>C	ENSP00000425596.1:p.Gly1155Ala
ENST00000619499.4:c.3560G>C	ENSP00000482132.1:p.Gly1187Ala
NM_001999.3:c.3563G>C	NP_001990.2:p.Gly1188Ala
XM_017009228.2:c.3410G>C	XP_016864717.1:p.Gly1137Ala
NM_001999.4:c.3563G>C MANE Select	NP_001990.2:p.Gly1188Ala